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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


In Mondo Disease Ontology:
MONDO:0013259 - Oguchi disease-2

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : grk1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hereditary night blindness (is_a)