DISEASES

Disease-gene associations mined from literature

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