Human genes for congenital stationary night blindness 1B
Congenital stationary night blindness 1B [DOID:0110865]
A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35.
Synonyms: congenital stationary night blindness 1B, DOID:0110865, autosomal recessive complete congenital stationary night blindness, congenital stationary night blindness 1B autosomal recessive, CSNB1B ...