has material basis in germline mutation in NYX congenital stationary night blindness 1A https://github.com/monarch-initiative/mondo/issues/4069 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4937 https://github.com/monarch-initiative/mondo/issues/5693 https://github.com/monarch-initiative/mondo/issues/7924 https://www.malacards.org/card/night_blindness_congenital_stationary_type_1a myopia-night blindness congenital stationary night blindness type 1A congenital stationary night blindness caused by mutation in NYX NYX congenital stationary night blindness night blindness, congenital stationary (complete), 1A, X-linked, X-linked recessive MONDO:0010690 night blindness, congenital stationary, type 1A GARD:0015306 DOID:0110870 CSNB1A hemeralopia-myopia UMLS:C3495587 NYX-related congenital stationary night blindness MEDGEN:501208 OMIM:310500 A congenital stationary night blindness caused by variants in the X-linked NYX gene. congenital stationary night blindness X-linked congenital stationary night blindness NYX-related retinopathy