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Disease Ontology Browser
Leber congenital amaurosis 19 (DOID:0081169)
Alliance: disease page
Alt IDs: OMIM:618513
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the USP45 gene on chromosome 6q16.

Disease References using Mouse Models (1)
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