| Descriptor English: | Glycogen Storage Disease Type V | ||||||
| Descriptor Spanish: |
Enfermedad del Almacenamiento de Glucógeno Tipo V
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| Descriptor Portuguese: | Doença de Depósito de Glicogênio Tipo V | ||||||
| Descriptor French: | Glycogénose de type V | ||||||
| Entry term(s): |
Deficiencies, Muscle Phosphorylase Deficiencies, PYGM Deficiency, Muscle Phosphorylase Deficiency, PYGM Disease, McArdle Disease, McArdle's Glycogen Storage Disease Type 5 Glycogen Storage Disease V Glycogenosis 5 Glycogenosis 5s McArdle Disease McArdle Type Glycogen Storage Disease McArdle's Disease McArdles Disease Mcardle Syndrome Mcardle Syndromes Muscle Glycogen Phosphorylase Deficiency Muscle Phosphorylase Deficiencies Muscle Phosphorylase Deficiency Myophosphorylase deficiencies Myophosphorylase deficiency PYGM Deficiencies PYGM Deficiency Phosphorylase Deficiencies, Muscle Phosphorylase Deficiency, Muscle Syndrome, Mcardle Syndromes, Mcardle deficiencies, Myophosphorylase deficiency, Myophosphorylase |
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| Tree number(s): |
C16.320.565.202.449.560 C18.452.648.202.449.560 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006012 | ||||||
| Scope note: | Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise. |
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| Annotation: | 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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| Previous Indexing: |
Glucosyltransferases/metabolism (1966-1974) Glycogenosis (1966-1974) Muscular Diseases (1966-1974) |
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| Public MeSH Note: | 1989; for GLYCOGENOSIS 5 see GLYCOGENOSIS 1975-1988 |
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| History Note: | 1989(1975); for GLYCOGENOSIS 5 use GLYCOGENOSIS 1975-1988 |
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| Entry Version: | GLYCOGEN STORAGE DIS V |
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| DeCS ID: | 24412 | ||||||
| Unique ID: | D006012 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1989/01/01 | ||||||
| Date of Entry: | 1974/12/12 | ||||||
| Revision Date: | 2013/07/08 |
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Glycogen Storage Disease Type V
- Preferred
| Concept UI |
M0009473 |
| Scope note | Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise. |
| Preferred term | Glycogen Storage Disease Type V |
| Entry term(s) |
Deficiencies, Muscle Phosphorylase Deficiencies, PYGM Deficiency, Muscle Phosphorylase Deficiency, PYGM Disease, McArdle Disease, McArdle's Glycogen Storage Disease Type 5 Glycogen Storage Disease V Glycogenosis 5 Glycogenosis 5s McArdle Disease McArdle Type Glycogen Storage Disease McArdle's Disease McArdles Disease Mcardle Syndrome Mcardle Syndromes Muscle Glycogen Phosphorylase Deficiency Muscle Phosphorylase Deficiencies Muscle Phosphorylase Deficiency Myophosphorylase deficiencies Myophosphorylase deficiency PYGM Deficiencies PYGM Deficiency Phosphorylase Deficiencies, Muscle Phosphorylase Deficiency, Muscle Syndrome, Mcardle Syndromes, Mcardle deficiencies, Myophosphorylase deficiency, Myophosphorylase |
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