OPN1MW, opsin 1, medium wave sensitive, 2652

N. diseases: 107; N. variants: 5
Disease: BORNHOLM EYE DISEASE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3159311
Disease: BORNHOLM EYE DISEASE
BORNHOLM EYE DISEASE 		0.300 GeneticVariation disease ORPHANET Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy. 23322568 2013