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DOID:0110714 - congenital stationary night blindness 1G
Disease Ontology Definition:A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the GNAT1 gene on chromosome 3p21.
Synonyms: CSNB1G, congenital stationary night blindness type 1G,
Xenbase Genes : gnat1
MONDO:0014614 - congenital stationary night blindness 1G |
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)