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

Xenbase Genes : nyx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010690 - manual digit 1 epithelium

MIM:
MIM:310500 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A

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

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