Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110870 - congenital stationary night blindness 1A

Disease Ontology Definition:A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.

Synonyms: CSNB1A, NBMI, complete CSNB X-linked, congenital stationary night blindness 1A X-linked, congenital stationary night blindness with myopia, hemeralopia-myopia, myopia-night blindness,

Xenbase Genes : nyx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010690 - congenital stationary night blindness 1A


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)