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Disease Ontology Browser
Leber congenital amaurosis (DOID:14791)
Alliance: disease page
Synonyms: LCA; Leber's amaurosis; Leber's congenital amaurosis; Leber's disease
Alt IDs: MESH:D057130, NCI:C129075, OMIM:PS204000, ORDO:65, UMLS_CUI:C0339527
Definition: A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness.

Disease References using Mouse Models (37)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
05/26/2020
MGI 6.15
The Jackson Laboratory