- Concept UI
- M0335588
- Scope Note
- A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
- Terms
-
Muscular Dystrophies, Limb-Girdle
Preferred Term
Term UI
T582097
Date04/08/2004
LexicalTag
NON
ThesaurusID
NLM (2005)
-
Limb-Girdle Muscular Dystrophies
Term UI
T582099
Date04/08/2004
LexicalTag
NON
ThesaurusID
NLM (2005)
-
Limb-Girdle Muscular Dystrophy
Term UI
T582098
Date04/08/2004
LexicalTag
NON
ThesaurusID
-
Muscular Dystrophy, Limb-Girdle
Term UI
T369182
Date11/08/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
Limb-Girdle Syndrome
Term UI
T841924
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Myopathic Limb-Girdle Syndrome
Term UI
T841925
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)