Human genes for congenital stationary night blindness 1A
Congenital stationary night blindness 1A [DOID:0110870]
A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.
Synonyms: congenital stationary night blindness 1A, DOID:0110870, complete CSNB X-linked, congenital stationary night blindness 1A X-linked, congenital stationary night blindness with myopia ...