Term Name:	congenital stationary night blindness 1D
Synonyms:	congenital stationary night blindness 1D autosomal recessive, CSNB1D
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22.
Ontology:	Human Disease [DOID:0110868]   (DOID:0110868)