NYX and Leber congenital amaurosis: This variant has been associated with several conditions: Congenital stationary night blindness, type 1A (CSNB1A) (MIM: 610445, inheritance: autosomal dominant [AD]); Retinitis pigmentosa, type 4 (RP4) (MIM: 613731, inheritance: [AD] or autosomal recessive [AR]); and Leber’s congenital amaurosis (LCA) (MIM: 136880, inheritance: [AD] or [AR]).