Term Name:	congenital stationary night blindness 1E
Synonyms:	congenital stationary night blindness 1E autosomal recessive, CSNB1E
Definition:	A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GPR179 gene on chromosome 17q12.
Ontology:	Human Disease [DOID:0110869]   ( DOID:0110869 )