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)

Relationships
is a type of: autosomal recessive disease congenital stationary night blindness