Term Name:	congenital stationary night blindness 1C
Synonyms:	congenital stationary night blindness 1C autosomal recessive, CSNB1C
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.
Ontology:	Human Disease [DOID:0110867]   ( DOID:0110867 )