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DOID:0110118 - Leber congenital amaurosis 16
Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the KCNJ13 gene on chromosome 2q37.
Synonyms: LCA16,
Xenbase Genes : kcnj13
MONDO:0013613 - Leber congenital amaurosis 16 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Leber congenital amaurosis (is_a)