Sarcoglycanopathies

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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	Sarcoglycanopathies Sarcoglycanopathies Sarcoglycanopathy 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".

Diseases [C]
Musculoskeletal Diseases [C05]
Muscular Diseases [C05.651]
Muscular Disorders, Atrophic [C05.651.534]
Muscular Dystrophies [C05.651.534.500]
Muscular Dystrophies, Limb-Girdle [C05.651.534.500.280]
Sarcoglycanopathies [C05.651.534.500.280.500]
Respiratory Tract Diseases [C08]
Respiration Disorders [C08.618]
Sarcoglycanopathies [C08.618.923]
Nervous System Diseases [C10]
Neuromuscular Diseases [C10.668]
Muscular Diseases [C10.668.491]
Muscular Disorders, Atrophic [C10.668.491.175]
Muscular Dystrophies [C10.668.491.175.500]
Muscular Dystrophies, Limb-Girdle [C10.668.491.175.500.149]
Sarcoglycanopathies [C10.668.491.175.500.149.500]
Cardiovascular Diseases [C14]
Heart Diseases [C14.280]
Cardiomyopathies [C14.280.238]
Sarcoglycanopathies [C14.280.238.812]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Muscular Dystrophies [C16.320.577]
Muscular Dystrophies, Limb-Girdle [C16.320.577.280]
Sarcoglycanopathies [C16.320.577.280.500]

Below are MeSH descriptors whose meaning is related to "Sarcoglycanopathies".

Below are MeSH descriptors whose meaning is more specific than "Sarcoglycanopathies".

publications

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