DOID:14791 - Leber congenital amaurosis
Disease Ontology Definition:A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness.
Synonyms: LCA, Leber's amaurosis, Leber's congenital amaurosis, Leber's disease
Xenbase Genes : crx, crb1, aipl1, spata7, impdh1, rpe65, iqcb1, kcnj13, nmnat1, lrat, pcyt1a, rd3, lca5, rpgrip1, gucy2d,
|MONDO:0018998 - Leber congenital amaurosis|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): physical disorder (is_a), retinal disease (is_a)