congenital stationary night blindness 1E

Summary

DOID:0110869 - congenital stationary night blindness 1E

Disease Ontology 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.

Synonyms: congenital stationary night blindness 1E autosomal recessive, CSNB1E

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gpr179

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013807 - congenital stationary night blindness 1E

MONDO:0013807 - congenital stationary night blindness 1E

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), congenital stationary night blindness (is_a)