Term Name:	congenital stationary night blindness 1B
Synonyms:	autosomal recessive complete congenital stationary night blindness, congenital stationary night blindness 1B autosomal recessive, CSNB1B
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35.
Ontology:	Human Disease [DOID:0110865]   ( DOID:0110865 )