Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55812
Gene Symbol: SPATA7
SPATA7
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		0.670 GermlineCausalMutation ORPHANET Review and update on the molecular basis of Leber congenital amaurosis. 25685757

2015
Entrez Id: 55812
Gene Symbol: SPATA7
SPATA7
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		0.670 GermlineCausalMutation ORPHANET Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. 19268277

2009