About   Help   FAQ
Disease Ontology Browser
Leber congenital amaurosis 9 (DOID:0110005)
Alliance: disease page
Synonyms: LCA9
Alt IDs: OMIM:608553, ICD10CM:H35.5
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36.

Disease References using Mouse Models (2)

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 Notice
Send questions and comments to User Support.
last database update
MGI 6.20
The Jackson Laboratory