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Glycogen Storage Disease MeSH Descriptor Data 2021


MeSH Heading
Glycogen Storage Disease
Tree Number(s)
C16.320.565.202.449
C18.452.648.202.449
Unique ID
D006008
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006008
Annotation
an inborn error of carbohydrate metab; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note
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.
Entry Version
GLYCOGEN STORAGE DIS
Entry Term(s)
Glycogenosis
NLM Classification #
QU 265.5.C3
Public MeSH Note
89; was GLYCOGENOSIS 1963-88
Online Note
use GLYCOGEN STORAGE DISEASE to search GLYCOGENOSIS 1966-88
History Note
89; was GLYCOGENOSIS 1963-88
Date Established
1989/01/01
Date of Entry
1999/01/01
Revision Date
2006/07/05
Glycogen Storage Disease Preferred
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