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: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.650 GermlineCausalMutation ORPHANET Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. 19268277

2009