congenital stationary night blindness 1F (DOID:0110864)
Alliance: disease page
Synonyms: congenital stationary night blindness 1F autosomal recessive; CSNB1F
Alt IDs: OMIM:615058
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25.