Limb-girdle muscular dystrophy, type 2C [Supplementary Concept]
Date introduced: August 25, 2010
MeSH Unique ID: C535900
Heading Mapped to:
Entry Terms:
- Duchenne-like muscular dystrophy, autosomal recessive, type 1
- Gamma-sarcoglycanopathy
- Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency
- SCARMD
- Muscular dystrophy, Duchenne-like
- Severe childhood autosomal recessive muscular dystrophy, North African type
- Muscular Dystrophy, Limb-Girdle, Type 2C
- LGMD2C
- Adhalin deficiency, secondary
- Maghrebian myopathy