About   Help   FAQ
Disease Ontology Browser
Leber congenital amaurosis 12 (DOID:0110080)
Alliance: disease page
Synonyms: LCA12
Alt IDs: OMIM:610612, ICD10CM:H35.5, MESH:C565697
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32.

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, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
01/24/2023
MGI 6.22
The Jackson Laboratory