congenital stationary night blindness 1E (DOID:0110869)
Alliance: disease page
Synonyms: congenital stationary night blindness 1E autosomal recessive; CSNB1E
Alt IDs: OMIM:614565
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GPR179 gene on chromosome 17q12.