Human genes for congenital stationary night blindness 1H
Congenital stationary night blindness 1H [DOID:0110866]
A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13.
Synonyms: congenital stationary night blindness 1H, DOID:0110866, congenital stationary night blindness type 1H, CSNB1H