MeSH Browser

MeSH Supplementary: Dysferlinopathy
Unique ID: C537995
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537995
Registry Numbers: 0
Heading Mapped to: *Muscular Dystrophies, Limb-Girdle
Frequency: 129
Note: Muscular dystrophy caused by mutations in the dysferlin (DYSF) gene, including limb-girdle muscular dystrophy type 2B, Miyoshi myopathy, and distal anterior compartment myopathy. OMIM: 603009
Date of Entry: 2010/08/25
Revision Date: 2016/08/01

Dysferlinopathy MeSH Supplementary Concept Data 2025