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Summary Literature (0)
DOID:0110713 - Oguchi disease-2

Disease Ontology Definition:A hereditary 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: CSNBO2, congenital stationary night blindness Oguchi type 2,

Xenbase Genes : grk1

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


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

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