Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 145226
Gene Symbol: RDH12
RDH12
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		0.500 GermlineCausalMutation ORPHANET Review and update on the molecular basis of Leber congenital amaurosis. 25685757

2015
Entrez Id: 145226
Gene Symbol: RDH12
RDH12
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		0.500 GermlineCausalMutation ORPHANET Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis. 15322982

2004