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DOID:0110016 - Leber congenital amaurosis 2
Disease Ontology Definition:A Leber congenital amaurosis that is characterized by night blindness, some transient improvement in vision, and eventual progressive visual loss and has_material_basis_in mutation in the RPE65 gene on chromosome 1.
Synonyms: LCA2, amaurosis congenita of Leber II,
Echinobase Genes :
MIM:204100 - leber congenital amaurosis 2; lca2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee