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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
3635	INPP5D	C0035126	Reperfusion Injury	0.2	CTD_human
3635	INPP5D	C0023893	Liver Cirrhosis, Experimental	0.2	CTD_human
3635	INPP5D	C4085251	PAGET DISEASE OF BONE 2, EARLY-ONSET	0.08	MGD
3635	INPP5D	C0266929	Chronic Periodontitis	0.00273291246481375	LHGDN
3635	INPP5D	C0040336	Tobacco Use Disorder	0.002407028523288	GAD
3635	INPP5D	C0019196	Hepatitis C	0.002407028523288	GAD
3635	INPP5D	C0023467	Leukemia, Myelocytic, Acute	0.0010989071368524	BEFREE
3635	INPP5D	C0023418	leukemia	0.0005494535684262	BEFREE
3635	INPP5D	C0023473	Myeloid Leukemia, Chronic	0.0005494535684262	BEFREE
3635	INPP5D	C0027022	Myeloproliferative disease	0.0005494535684262	BEFREE
3635	INPP5D	C0598766	Leukemogenesis	0.0002747267842131	BEFREE
3635	INPP5D	C0085669	Acute leukemia	0.0002747267842131	BEFREE
3635	INPP5D	C0149896	Primary gout	0.0002747267842131	BEFREE
3635	INPP5D	C0239946	Fibrosis, Liver	0.0002747267842131	BEFREE
3635	INPP5D	C0280449	secondary acute myeloid leukemia	0.0002747267842131	BEFREE
3635	INPP5D	C0349639	Juvenile Myelomonocytic Leukemia	0.0002747267842131	BEFREE
3635	INPP5D	C0524910	Hepatitis C, Chronic	0.0002747267842131	BEFREE
3635	INPP5D	C0596263	Carcinogenesis	0.0002747267842131	BEFREE
3635	INPP5D	C0002395	Alzheimer's Disease	0.0002747267842131	BEFREE
3635	INPP5D	C0856825	Acute GVH disease	0.0002747267842131	BEFREE
3635	INPP5D	C1292778	Chronic myeloproliferative disorder	0.0002747267842131	BEFREE
3635	INPP5D	C1318020	Stromal keratitis	0.0002747267842131	BEFREE
3635	INPP5D	C1961099	Precursor T-Cell Lymphoblastic Leukemia-Lymphoma	0.0002747267842131	BEFREE
3635	INPP5D	C3463824	MYELODYSPLASTIC SYNDROME	0.0002747267842131	BEFREE
3635	INPP5D	C0004096	Asthma	0.0002747267842131	BEFREE
3635	INPP5D	C0079744	Diffuse Large B-Cell Lymphoma	0.0002747267842131	BEFREE
3635	INPP5D	C0079731	B-Cell Lymphomas	0.0002747267842131	BEFREE
3635	INPP5D	C0042769	Virus Diseases	0.0002747267842131	BEFREE
3635	INPP5D	C0038454	Cerebrovascular accident	0.0002747267842131	BEFREE
3635	INPP5D	C0003850	Arteriosclerosis	0.0002747267842131	BEFREE
3635	INPP5D	C0029408	Degenerative polyarthritis	0.0002747267842131	BEFREE
3635	INPP5D	C0028754	Obesity	0.0002747267842131	BEFREE
3635	INPP5D	C0026764	Multiple Myeloma	0.0002747267842131	BEFREE
3635	INPP5D	C0024299	Lymphoma	0.0002747267842131	BEFREE
3635	INPP5D	C0003873	Rheumatoid Arthritis	0.0002747267842131	BEFREE
3635	INPP5D	C0023470	Myeloid Leukemia	0.0002747267842131	BEFREE
3635	INPP5D	C0023449	Acute lymphocytic leukemia	0.0002747267842131	BEFREE
3635	INPP5D	C0018133	Graft-vs-Host Disease	0.0002747267842131	BEFREE
3635	INPP5D	C0010674	Cystic Fibrosis	0.0002747267842131	BEFREE
3635	INPP5D	C0010346	Crohn Disease	0.0002747267842131	BEFREE
3635	INPP5D	C0004153	Atherosclerosis	0.0002747267842131	BEFREE