MeSH Browser

MeSH Supplementary: Limb-girdle muscular dystrophy, type 2C
Unique ID: C535900
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535900
Entry Term(s): Adhalin deficiency, secondary; Duchenne-like muscular dystrophy, autosomal recessive, type 1; Gamma-sarcoglycanopathy; LGMD2C; Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency; Maghrebian myopathy; Muscular Dystrophy, Limb-Girdle, Type 2C; Muscular dystrophy, Duchenne-like; SCARMD; Severe childhood autosomal recessive muscular dystrophy, North African type
Registry Numbers: 0
Heading Mapped to: *Sarcoglycanopathies
Frequency: 15
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Limb-girdle muscular dystrophy, type 2C MeSH Supplementary Concept Data 2025