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Summary Literature (0)
DOID:0060255 - rippling muscle disease 2

Disease Ontology 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.

Synonyms: autosomal dominant limb-girdle muscular dystrophy type 1C

Xenbase Genes : cav3, cav3.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019947 - rippling muscle disease 2

MIM:
MIM:606072 - RIPPLING MUSCLE DISEASE 2; RMD2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), muscle tissue disease (is_a)