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DOID:0081169 - Leber congenital amaurosis 19
Disease Ontology Definition:A Leber congenital amaurosis that has_material_basis_in mutation in the USP45 gene on chromosome 6q16.
Synonyms:
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Leber congenital amaurosis (is_a)