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:0110712 - Oguchi disease-1


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 or compound heterozygous mutation in the SAG gene on chromosome 2q37.

Synonyms: CSNBO1, congenital stationary night blindness Oguchi type 1

In OMIM:
OMIM:258100 - OGUCHI DISEASE 1

In Mondo Disease Ontology:
MONDO:0009775 - Oguchi disease-1

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

Xenbase Genes : sag, grk1

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