Matches were found for CACNA1F (Night Blindness, congenital, stationary, X-linked, Type 2- CSNB2; OMIM 300071), GNAT1 (Night Blindness, congenital, stationary, autosomal dominant 3-CSNBAD3; OMIM 610444), RHO (Retinitis pigmentosa 4-RP4; OMIM 180380; also, Night Blindness, congenital, stationary, autosomal dominant 1-CSNBAD1; OMIM 610445), and OAT (Gyrate atrophy; OMIM 258870). This evidence concerns the gene OAT and Gyrate atrophy of choroid and retina.