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Sarcoglycanopathies MeSH Descriptor Data 2024


MeSH Heading
Sarcoglycanopathies
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
Unique ID
D058088
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D058088
Scope Note
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.
Entry Term(s)
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
Sarcoglycanopathy
Public MeSH Note
2011
History Note
2011
Date Established
2011/01/01
Date of Entry
2010/06/25
Revision Date
2013/07/08
Sarcoglycanopathies Preferred
Alpha-Sarcoglycanopathies Narrower
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