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Summary Literature (0)
DOID:0110866 - congenital stationary night blindness 1H

Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13.

Synonyms: CSNB1H, congenital stationary night blindness type 1H,

Xenbase Genes : gnb3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014872 - congenital stationary night blindness 1H


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

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