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Summary Literature (0)
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 : gnat1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012497 - congenital stationary night blindness autosomal dominant 3

OMIM:
OMIM:610444 - NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital stationary night blindness (is_a)