congenital stationary night blindness 1C (DOID:0110867)
Alliance: disease page
Synonyms: congenital stationary night blindness 1C autosomal recessive; CSNB1C
Alt IDs: OMIM:613216
Definition: A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14.