"Sarcoglycanopathies" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D058088
|
| MeSH Number(s) |
C05.651.534.500.280.500 C08.618.923 C10.668.491.175.500.149.500 C14.280.238.812 C16.320.577.280.500
|
| Concept/Terms |
Alpha-Sarcoglycanopathies- Alpha-Sarcoglycanopathies
- Alpha Sarcoglycanopathies
- Adhalinopathy, Primary
- Adhalinopathies, Primary
- Primary Adhalinopathies
- Primary Adhalinopathy
- LGMD2D
- Muscular Dystrophy Limb-Girdle with Alpha-Sarcoglycan Deficiency
- Muscular Dystrophy Limb Girdle with Alpha Sarcoglycan Deficiency
- Limb-Girdle Muscular Dystrophy, Type 2D
- Limb Girdle Muscular Dystrophy, Type 2D
- Alpha-Sarcoglycanopathy
- Alpha Sarcoglycanopathy
- Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2
- Duchenne Like Autosomal Recessive Muscular Dystrophy, Type 2
- Adhalinopathies
- Muscular Dystrophy, Limb-Girdle, Type 2D
|
Below are MeSH descriptors whose meaning is more general than "Sarcoglycanopathies".
Below are MeSH descriptors whose meaning is more specific than "Sarcoglycanopathies".
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Below are the most recent publications written about "Sarcoglycanopathies" by people in Profiles.
MeSH information
