congenital stationary night blindness 1D (DOID:0110868)
Alliance: disease page
Synonyms: congenital stationary night blindness 1D autosomal recessive; CSNB1D
Alt IDs: OMIM:613830
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22.