Gene: RDH12 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 145226
Gene Symbol: RDH12
RDH12 		0.120 Biomarker disease BEFREE RDH12-IRD causes an early-onset, retina-wide disease with particularly severe central retinal abnormalities associated with relatively less severe rod photoreceptor dysfunction, a pattern consistent with an early-onset cone-rod dystrophy. 30372751 2018
Entrez Id: 145226
Gene Symbol: RDH12
RDH12 		0.120 GeneticVariation disease BEFREE Novel RDH12 mutations associated with Leber congenital amaurosis and cone-rod dystrophy: biochemical and clinical evaluations. 17512964 2007
Entrez Id: 145226
Gene Symbol: RDH12
RDH12 		0.120 GeneticVariation disease CLINVAR