"Glycogen Storage Disease" 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.
A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| Descriptor ID |
D006008
|
| MeSH Number(s) |
C16.320.565.202.449 C18.452.648.202.449
|
| Concept/Terms |
Glycogen Storage Disease- Glycogen Storage Disease
- Disease, Glycogen Storage
- Diseases, Glycogen Storage
- Glycogen Storage Diseases
- Storage Disease, Glycogen
- Storage Diseases, Glycogen
- Glycogenosis
- Glycogenoses
|
Below are MeSH descriptors whose meaning is more general than "Glycogen Storage Disease".
Below are MeSH descriptors whose meaning is more specific than "Glycogen Storage Disease".
This graph shows the total number of publications written about "Glycogen Storage Disease" by people in this website by year, and whether "Glycogen Storage Disease" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 |
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Below are the most recent publications written about "Glycogen Storage Disease" by people in Profiles.
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Glycogenic hepatopathy: an underrecognized hepatic complication of diabetes mellitus. Am J Surg Pathol. 2006 Apr; 30(4):508-13.
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Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study. Isr J Med Sci. 1990 Jun; 26(6):328-33.