Term Name:	congenital stationary night blindness autosomal dominant 1
Synonyms:	CSNBAD1, rhodopsin-related congenital stationary night blindness
Definition:	A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1.
Ontology:	Human Disease [DOID:0110862]   ( DOID:0110862 )