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Disease Ontology Browser
Leber congenital amaurosis 2 (DOID:0110016)
Alliance: disease page
Synonyms: amaurosis congenita of Leber II; LCA2
Alt IDs: OMIM:204100, ICD10CM:H35.5
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.

Disease References using Mouse Models (10)
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory