congenital stationary night blindness 1B (DOID:0110865)
Alliance: disease page
Synonyms: autosomal recessive complete congenital stationary night blindness; congenital stationary night blindness 1B autosomal recessive; CSNB1B
Alt IDs: OMIM:257270
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35.