"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".
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MeSH information
