Term Name:	congenital stationary night blindness 1G
Synonyms:	congenital stationary night blindness type 1G, CSNB1G
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the GNAT1 gene on chromosome 3p21.
Ontology:	Human Disease [DOID:0110714]   ( DOID:0110714 )