Human genes for congenital stationary night blindness 1C
Congenital stationary night blindness 1C [DOID:0110867]
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.
Synonyms: congenital stationary night blindness 1C, DOID:0110867, congenital stationary night blindness 1C autosomal recessive, CSNB1C