Human genes for congenital stationary night blindness autosomal dominant 1
Congenital stationary night blindness autosomal dominant 1 [DOID:0110862]
A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1.
Synonyms: congenital stationary night blindness autosomal dominant 1, DOID:0110862, CSNBAD1, rhodopsin-related congenital stationary night blindness, rhodopsinrelated congenital stationary night blindness ...