|
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:0014872 - congenital stationary night blindness 1H |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee