Sarcoglycanopathies
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.
Year introduced: 2011
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Subheadings:
Tree 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
MeSH Unique ID: D058088
Entry Terms:
- Sarcoglycanopathy
- Alpha-Sarcoglycanopathies
- Alpha Sarcoglycanopathies
- Adhalinopathy, Primary
- Adhalinopathies, Primary
- Primary Adhalinopathies
- Primary Adhalinopathy
- LGMD2D
- Muscular Dystrophy, Limb-Girdle, Type 2D
- 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 with Alpha-Sarcoglycan Deficiency
- Muscular Dystrophy Limb Girdle with Alpha Sarcoglycan Deficiency