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Summary Literature (0)
DOID:0110871 - congenital stationary night blindness 2A

Disease Ontology Definition:A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23.

Synonyms: congenital stationary night blindness 2A X-linked

Xenbase Genes : cacna1f

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010241 - congenital stationary night blindness 2A


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)