Descriptor English: | Glycogen Storage Disease | ||||||
Descriptor Spanish: |
Enfermedad del Almacenamiento de Glucógeno
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Descriptor Portuguese: | Doença de Depósito de Glicogênio | ||||||
Descriptor French: | Glycogénose | ||||||
Entry term(s): |
Disease, Glycogen Storage Diseases, Glycogen Storage Glycogen Storage Diseases Glycogenoses Glycogenosis Storage Disease, Glycogen Storage Diseases, Glycogen |
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Tree number(s): |
C16.320.565.202.449 C18.452.648.202.449 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006008 | ||||||
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. |
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Annotation: | an inborn error of carbohydrate metab; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Public MeSH Note: | 89; was GLYCOGENOSIS 1963-88 |
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Online Note: | use GLYCOGEN STORAGE DISEASE to search GLYCOGENOSIS 1966-88 |
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History Note: | 89; was GLYCOGENOSIS 1963-88 |
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Entry Version: | GLYCOGEN STORAGE DIS |
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DeCS ID: | 24388 | ||||||
Unique ID: | D006008 | ||||||
NLM Classification: | WD 205.5.C2 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1989/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2006/07/05 |
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Glycogen Storage Disease
- Preferred
Concept UI |
M0009469 |
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. |
Preferred term | Glycogen Storage Disease |
Entry term(s) |
Disease, Glycogen Storage Diseases, Glycogen Storage Glycogen Storage Diseases Glycogenoses Glycogenosis Storage Disease, Glycogen Storage Diseases, Glycogen |
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