DISEASES

Disease-gene associations mined from literature

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