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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
56623	INPP5E	C0431399	Familial aplasia of the vermis	0.601648360705279	BEFREE;CTD_human;ORPHANET;UNIPROT
56623	INPP5E	C1857802	MORM syndrome	0.400274726784213	BEFREE;CTD_human;ORPHANET
56623	INPP5E	C0015398	Eye Diseases, Hereditary	0.2	CTD_human
56623	INPP5E	C0008780	Ciliary Motility Disorders	0.2	CTD_human
56623	INPP5E	C0028754	Obesity	0.2	CTD_human
56623	INPP5E	C4274118	Joubert syndrome with ocular defect	0.2	ORPHANET
56623	INPP5E	C0030846	Penile Diseases	0.2	CTD_human
56623	INPP5E	C3714756	Intellectual Disability	0.2	CTD_human
56623	INPP5E	C1857662	COACH syndrome	0.2	ORPHANET
56623	INPP5E	C4277690	Ciliopathies	0.0008241803526393	BEFREE
56623	INPP5E	C0028860	Oculocerebrorenal Syndrome	0.0008241803526393	BEFREE
56623	INPP5E	C0878681	Dent's disease	0.0002747267842131	BEFREE
56623	INPP5E	C0752166	Bardet-Biedl Syndrome	0.0002747267842131	BEFREE
56623	INPP5E	C0266464	Polymicrogyria	0.0002747267842131	BEFREE
56623	INPP5E	C3714506	Meckel syndrome type 1	0.0002747267842131	BEFREE
56623	INPP5E	C0152427	Polydactyly	0.0002747267842131	BEFREE
56623	INPP5E	C3887499	Renal cyst	0.0002747267842131	BEFREE
56623	INPP5E	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0002747267842131	BEFREE
56623	INPP5E	C0025202	melanoma	0.0002747267842131	BEFREE