Gene: RPE65 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6121
Gene Symbol: RPE65
RPE65 		0.110 GeneticVariation disease BEFREE Individuals affected with LCA are diagnosed at birth or in the first few months of life with severely impaired vision or blindness, nystagmus and an abnormal or flat electroretinogram (ERG).Mutations in GUCY2D (ref.3), RPE65 (ref.4) and CRX (ref. 10615133 2000
Entrez Id: 6121
Gene Symbol: RPE65
RPE65 		0.110 Biomarker disease HPO