Structured Summary
Abstract
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.
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MeSH Record
Synonyms
7 entry terms
- Glycogenosis
- Disease, Glycogen Storage
- Diseases, Glycogen Storage
- Glycogen Storage Diseases
- Glycogenoses
- Storage Disease, Glycogen
- Storage Diseases, Glycogen
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
an inborn error of carbohydrate metab; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
MeSH Record
History Note
89; was GLYCOGENOSIS 1963-88
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NLM Classification
QU 265.5.C3
AMA Style
References
- National Library of Medicine. Glycogen Storage Disease. Medical Subject Headings (MeSH). 2026. Unique ID D006008. http://id.nlm.nih.gov/mesh/2026/D006008
- Glycogen Storage Disease. In: Wikipedia. https://en.wikipedia.org/wiki/Glycogen_storage_disease
- Glycogen Storage Disease. In: Wikidata. https://www.wikidata.org/wiki/Q1421738