* We recommend a score >= 0.08 for meaningful Gene-Disease associations

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
2538	G6PC	C0017920	Glycogen Storage Disease Type I	0.697502646277691	BEFREE;CTD_human;GAD;LHGDN;MGD;ORPHANET;UNIPROT
2538	G6PC	C2919796	Glycogen storage disease type Ia	0.20796707674218	BEFREE;CTD_human
2538	G6PC	C2239176	Liver carcinoma	0.20685381422801	BEFREE;HPO;LHGDN
2538	G6PC	C0020615	Hypoglycemia	0.201923087489492	BEFREE;HPO
2538	G6PC	C0001125	Acidosis, Lactic	0.2	HPO
2538	G6PC	C0003868	Arthritis, Gouty	0.2	HPO
2538	G6PC	C0017668	Focal glomerulosclerosis	0.2	HPO
2538	G6PC	C0018099	Gout	0.2	HPO
2538	G6PC	C0019209	Hepatomegaly	0.2	HPO
2538	G6PC	C0020473	Hyperlipidemia	0.2	HPO
2538	G6PC	C0020538	Hypertensive disease	0.2	HPO
2538	G6PC	C0023893	Liver Cirrhosis, Experimental	0.2	CTD_human
2538	G6PC	C0029456	Osteoporosis	0.2	HPO
2538	G6PC	C0030305	Pancreatitis	0.2	HPO
2538	G6PC	C0033687	Proteinuria	0.2	HPO
2538	G6PC	C0034012	Delayed Puberty	0.2	HPO
2538	G6PC	C0043325	Xanthomatosis	0.2	HPO
2538	G6PC	C0086565	Liver Dysfunction	0.2	HPO
2538	G6PC	C0151766	Liver function tests abnormal finding	0.2	HPO
2538	G6PC	C0235996	Hepatic enzyme increased	0.2	HPO
2538	G6PC	C0239181	Intermittent diarrhea	0.2	HPO
2538	G6PC	C0339477	Lipidemia retinalis	0.2	HPO
2538	G6PC	C0347959	Lactic acidemia	0.2	HPO
2538	G6PC	C0349588	Short stature	0.2	HPO
2538	G6PC	C0392525	Nephrolithiasis	0.2	HPO
2538	G6PC	C0438237	Liver enzymes abnormal	0.2	HPO
2538	G6PC	C0438717	Transaminases increased	0.2	HPO
2538	G6PC	C0497247	Increase in blood pressure	0.2	HPO
2538	G6PC	C0542518	Enlarged kidney	0.2	HPO
2538	G6PC	C0853068	Glomerular filtration rate decreased	0.2	HPO
2538	G6PC	C0877359	Liver function test increased	0.2	HPO
2538	G6PC	C1458140	Bleeding tendency	0.2	HPO
2538	G6PC	C1837108	Decreased muscle mass	0.2	HPO
2538	G6PC	C1842003	Subclinical abnormal liver function tests	0.2	HPO
2538	G6PC	C1848701	Elevated hepatic transaminases	0.2	HPO
2538	G6PC	C1854928	Protuberant abdomen	0.2	HPO
2538	G6PC	C1856361	Doll-like facies	0.2	HPO
2538	G6PC	C1862761	Increased hepatocellular carcinoma risk	0.2	HPO
2538	G6PC	C1867955	Increased incidence of hepatocellular carcinoma	0.2	HPO
2538	G6PC	C4020899	Autosomal recessive predisposition	0.2	HPO
2538	G6PC	C0017919	Glycogen Storage Disease	0.0188619248214395	BEFREE;GAD;LHGDN
2538	G6PC	C0268146	Glucose-6-phosphate transport defect	0.0041209017631965	BEFREE
2538	G6PC	C0023903	Liver neoplasms	0.0035714481947703	BEFREE
2538	G6PC	C0038644	Sudden infant death syndrome	0.00328236603323995	BEFREE;LHGDN
2538	G6PC	C0011854	Diabetes Mellitus, Insulin-Dependent	0.0029564820917142	BEFREE;GAD
2538	G6PC	C0017495	Gerstmann-Straussler-Scheinker Disease	0.002747267842131	BEFREE
2538	G6PC	C0029438	Massive Osteolyses	0.002747267842131	BEFREE
2538	G6PC	C0025517	Metabolic Diseases	0.0019230874894917	BEFREE
2538	G6PC	C2711227	Steatohepatitis	0.0013736339210655	BEFREE
2538	G6PC	C0020456	Hyperglycemia	0.0010989071368524	BEFREE
2538	G6PC	C0206669	Hepatocellular Adenoma	0.0010989071368524	BEFREE
2538	G6PC	C0001430	Adenoma	0.0008241803526393	BEFREE
2538	G6PC	C0006118	Brain Neoplasms	0.0008241803526393	BEFREE
2538	G6PC	C0011847	Diabetes	0.0008241803526393	BEFREE
2538	G6PC	C0011849	Diabetes Mellitus	0.0008241803526393	BEFREE
2538	G6PC	C0011860	Diabetes Mellitus, Non-Insulin-Dependent	0.0008241803526393	BEFREE
2538	G6PC	C0015695	Fatty Liver	0.0008241803526393	BEFREE
2538	G6PC	C0017922	Glycogen Storage Disease Type III	0.0008241803526393	BEFREE
2538	G6PC	C0022658	Kidney Diseases	0.0008241803526393	BEFREE
2538	G6PC	C0271708	Fasting Hypoglycemia	0.0008241803526393	BEFREE
2538	G6PC	C0340970	Congenital neutropenia	0.0008241803526393	BEFREE
2538	G6PC	C1853118	Severe congenital neutropenia	0.0008241803526393	BEFREE
2538	G6PC	C3899988	Autosomal Recessive Disorder	0.0008241803526393	BEFREE
2538	G6PC	C0017636	Glioblastoma	0.0005494535684262	BEFREE
2538	G6PC	C0021294	Infant, Premature	0.0005494535684262	BEFREE
2538	G6PC	C0268147	Glycogen storage disease, type IX	0.0005494535684262	BEFREE
2538	G6PC	C0271650	Impaired glucose tolerance	0.0005494535684262	BEFREE
2538	G6PC	C0001627	Congenital adrenal hyperplasia	0.0002747267842131	BEFREE
2538	G6PC	C0007134	Renal Cell Carcinoma	0.0002747267842131	BEFREE
2538	G6PC	C0017638	Glioma	0.0002747267842131	BEFREE
2538	G6PC	C0017921	Glycogen storage disease type II	0.0002747267842131	BEFREE
2538	G6PC	C0017927	Glycogen Storage Disease Type VIII	0.0002747267842131	BEFREE
2538	G6PC	C0019196	Hepatitis C	0.0002747267842131	BEFREE
2538	G6PC	C0020443	Hypercholesterolemia	0.0002747267842131	BEFREE
2538	G6PC	C0020459	Hyperinsulinism	0.0002747267842131	BEFREE
2538	G6PC	C0021670	insulinoma	0.0002747267842131	BEFREE
2538	G6PC	C0021831	Intestinal Diseases	0.0002747267842131	BEFREE
2538	G6PC	C0023530	Leukopenia	0.0002747267842131	BEFREE
2538	G6PC	C0023895	Liver diseases	0.0002747267842131	BEFREE
2538	G6PC	C0027022	Myeloproliferative disease	0.0002747267842131	BEFREE
2538	G6PC	C0027819	Neuroblastoma	0.0002747267842131	BEFREE
2538	G6PC	C0027947	Neutropenia	0.0002747267842131	BEFREE
2538	G6PC	C0029925	Ovarian Carcinoma	0.0002747267842131	BEFREE
2538	G6PC	C0032460	Polycystic Ovary Syndrome	0.0002747267842131	BEFREE
2538	G6PC	C0035078	Kidney Failure	0.0002747267842131	BEFREE
2538	G6PC	C0242339	Dyslipidemias	0.0002747267842131	BEFREE
2538	G6PC	C0342492	Adrenal hypertrophy or hyperplasia	0.0002747267842131	BEFREE
2538	G6PC	C0342751	Generalized glycogen storage disease of infants	0.0002747267842131	BEFREE
2538	G6PC	C0700095	Central neuroblastoma	0.0002747267842131	BEFREE
2538	G6PC	C0740394	Hyperuricemia	0.0002747267842131	BEFREE
2538	G6PC	C0851887	Adenoviral infections	0.0002747267842131	BEFREE
2538	G6PC	C1140680	Malignant neoplasm of ovary	0.0002747267842131	BEFREE
2538	G6PC	C1291390	Deficiency of phosphorylase kinase	0.0002747267842131	BEFREE
2538	G6PC	C1512409	Hepatocarcinogenesis	0.0002747267842131	BEFREE
2538	G6PC	C1565489	Renal Insufficiency	0.0002747267842131	BEFREE
2538	G6PC	C1621895	Adrenal hyperplasia	0.0002747267842131	BEFREE
2538	G6PC	C1955741	Glucocorticoid deficiency	0.0002747267842131	BEFREE
2538	G6PC	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0002747267842131	BEFREE