Structured Summary
Abstract
Deficiencies or mutations in the genes for the SARCOGLYCAN COMPLEX subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency.
MeSH Record
Classification
Related Concepts
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MeSH Record
Synonyms
18 entry terms
- Sarcoglycanopathy
- Adhalinopathies
- Adhalinopathy, Primary
- Alpha-Sarcoglycanopathies
- Alpha-Sarcoglycanopathy
- Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2
- LGMD2D
- Limb-Girdle Muscular Dystrophy, Type 2D
- Muscular Dystrophy Limb-Girdle with Alpha-Sarcoglycan Deficiency
- Muscular Dystrophy, Limb-Girdle, Type 2D
- Adhalinopathies, Primary
- Alpha Sarcoglycanopathies
- Alpha Sarcoglycanopathy
- Duchenne Like Autosomal Recessive Muscular Dystrophy, Type 2
- Limb Girdle Muscular Dystrophy, Type 2D
- Muscular Dystrophy Limb Girdle with Alpha Sarcoglycan Deficiency
- Primary Adhalinopathies
- Primary Adhalinopathy
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2011
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Sarcoglycanopathies. Medical Subject Headings (MeSH). 2026. Unique ID D058088. http://id.nlm.nih.gov/mesh/2026/D058088
- Sarcoglycanopathies. In: Wikipedia. https://en.wikipedia.org/wiki/Sarcoglycanopathy
- Sarcoglycanopathies. In: Wikidata. https://www.wikidata.org/wiki/Q7423586