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:0110713 - Oguchi disease-2

Disease Ontology Definition:A congenital stationary night blindness characterized by congenital static night blindness, a golden or gray-white discoloration of the fundus that disappears in the dark-adapted state and typically normal function of all other visual functions that has_material_basis_in homozygous mutation in the GRK1 gene on chromosome 13q34.

Synonyms: congenital stationary night blindness Oguchi type 2, CSNBO2

Xenbase Genes : grk1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013259 - Oguchi disease-2


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

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