congenital stationary night blindness autosomal dominant 3

Summary

DOID:0110715 - congenital stationary night blindness autosomal dominant 3

Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21.

Synonyms: CSNBAD3, Nougaret type congenital stationary night blindness

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

: gnat1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012497 - congenital stationary night blindness autosomal dominant 3

MONDO:0012497 - congenital stationary night blindness autosomal dominant 3

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

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

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