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Disease Ontology Browser
Leber congenital amaurosis 2 (DOID:0110016)
Synonyms: amaurosis congenita of Leber II; LCA2
Alt IDs: OMIM:204100, ICD10CM:H35.5, ORDO:65
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/18/2017
MGI 6.08
The Jackson Laboratory