About   Help   FAQ
Disease Ontology Browser
autosomal dominant limb-girdle muscular dystrophy type 1C (DOID:0110302)
Alliance: disease page
Synonyms: LGMD1C; limb-girdle muscular dystrophy due to caveolin-3 deficiency; muscular dystrophy limb-girdle type IC
Alt IDs: OMIM:607801, ICD10CM:G71.0, ORDO:265
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in mutation in the caveolin-3 gene (CAV3) on chromosome 3p25.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.11
The Jackson Laboratory