Glycogen Storage Disease Type IIb
"Glycogen Storage Disease Type IIb" 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.
An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene encoding LYSOSOMAL-ASSOCIATED MEMBRANE PROTEIN 2.
| Descriptor ID |
D052120
|
| MeSH Number(s) |
C10.597.606.643.455.562 C14.280.238.458 C16.320.322.201 C16.320.565.202.449.510 C18.452.648.202.449.510
|
| Concept/Terms |
Glycogen Storage Disease Type IIb- Glycogen Storage Disease Type IIb
- Danon Disease
- Glycogen Storage Cardiomyopathy
- Cardiomyopathies, Glycogen Storage
- Cardiomyopathy, Glycogen Storage
- Glycogen Storage Cardiomyopathies
- Glycogen Storage Disease IIb
- Glycogen Storage Disease Limited to the Heart
- Lysosomal Glycogen Storage Disease with Normal Acid Maltase
- Lysosomal Glycogen Storage Disease without Acid Maltase Deficiency
- Pseudoglycogenosis 2
- Pseudoglycogenosis 2s
- Pseudoglycogenosis II
- Pseudoglycogenosis IIs
- Vacuolar Cardiomyopathy and Myopathy, X-linked
- Vacuolar Cardiomyopathy and Myopathy, X linked
- X-Linked Vacuolar Cardiomyopathy and Myopathy
- X Linked Vacuolar Cardiomyopathy and Myopathy
- Antopol Disease
- Disease, Antopol
- Glycogen Storage Disease Type 2B
|
Below are MeSH descriptors whose meaning is more general than "Glycogen Storage Disease Type IIb".
Below are MeSH descriptors whose meaning is more specific than "Glycogen Storage Disease Type IIb".
This graph shows the total number of publications written about "Glycogen Storage Disease Type IIb" by people in this website by year, and whether "Glycogen Storage Disease Type IIb" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
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Below are the most recent publications written about "Glycogen Storage Disease Type IIb" by people in Profiles.
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LAMP2 microdeletions in patients with Danon disease. Circ Cardiovasc Genet. 2010 Apr; 3(2):129-37.
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Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children. Circulation. 2005 Sep 13; 112(11):1612-7.