Human genes for congenital stationary night blindness autosomal dominant 3
Congenital stationary night blindness autosomal dominant 3 [DOID:0110715]
A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21.
Synonyms: congenital stationary night blindness autosomal dominant 3, DOID:0110715, CSNBAD3, Nougaret type congenital stationary night blindness, Nougaret type congenital stationary night blindnesses