rippling muscle disease 2 (DOID:0060255)
Alliance: disease page
Synonyms: autosomal dominant limb-girdle muscular dystrophy type 1C
Alt IDs: OMIM:606072, ORDO:265, ORDO:97238, UMLS_CUI:C1853698
Definition: A muscle tissue disease characterized by mechanically triggered contractions of skeletal muscle and that has_material_basis_in mutation in the caveolin-3 gene (CAV3) on chromosome 3p25.