Term Name:	congenital stationary night blindness autosomal dominant 3
Synonyms:	CSNBAD3, Nougaret type congenital stationary night blindness
Definition:	A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21.
Ontology:	Human Disease [DOID:0110715]   ( DOID:0110715 )