About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory