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Disease Ontology Browser
autosomal dominant limb-girdle muscular dystrophy type 1C (DOID:0110302)
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 (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/20/2017
MGI 6.10
The Jackson Laboratory