DISEASES

Disease-gene associations mined from literature

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,  CSNB1B,  autosomal recessive complete congenital stationary night blindness,  congenital stationary night blindness 1B autosomal recessive ...