MeSH Browser

MeSH Heading: Glycogen Storage Disease Type V
Tree Number(s): C16.320.565.202.449.560; C18.452.648.202.449.560
Unique ID: D006012
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D006012
Annotation: do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note: Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
Entry Version: GLYCOGEN STORAGE DIS V
Entry Term(s): Deficiency, Muscle Phosphorylase; Glycogen Storage Disease Type 5; Glycogen Storage Disease V; Glycogenosis 5; McArdle Disease; McArdle Type Glycogen Storage Disease; McArdle's Disease; Mcardle Syndrome; Muscle Glycogen Phosphorylase Deficiency; Muscle Phosphorylase Deficiency; Myophosphorylase deficiency; PYGM Deficiency
Previous Indexing: Glucosyltransferases/metabolism (1966-1974); Glycogenosis (1966-1974); Muscular Diseases (1966-1974)
Public MeSH Note: 1989; for GLYCOGENOSIS 5 see GLYCOGENOSIS 1975-1988
History Note: 1989(1975); for GLYCOGENOSIS 5 use GLYCOGENOSIS 1975-1988
Date Established: 1989/01/01
Date of Entry: 1974/12/12
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Metabolism, Inborn Errors [C16.320.565]
    - Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
      - Glycogen Storage Disease [C16.320.565.202.449]
        
        Glycogen Storage Disease Type I [C16.320.565.202.449.448]
        
        Glycogen Storage Disease Type II [C16.320.565.202.449.500]
        
        Glycogen Storage Disease Type IIb [C16.320.565.202.449.510]
        
        Glycogen Storage Disease Type III [C16.320.565.202.449.520]
        
        Glycogen Storage Disease Type IV [C16.320.565.202.449.540]
        
        Glycogen Storage Disease Type V [C16.320.565.202.449.560]
        
        Glycogen Storage Disease Type VI [C16.320.565.202.449.580]
        
        Glycogen Storage Disease Type VII [C16.320.565.202.449.600]
        
        Glycogen Storage Disease Type VIII [C16.320.565.202.449.620]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
      - Glycogen Storage Disease [C18.452.648.202.449]
        
        Glycogen Storage Disease Type I [C18.452.648.202.449.448]
        
        Glycogen Storage Disease Type II [C18.452.648.202.449.500]
        
        Glycogen Storage Disease Type IIb [C18.452.648.202.449.510]
        
        Glycogen Storage Disease Type III [C18.452.648.202.449.520]
        
        Glycogen Storage Disease Type IV [C18.452.648.202.449.540]
        
        Glycogen Storage Disease Type V [C18.452.648.202.449.560]
        
        Glycogen Storage Disease Type VI [C18.452.648.202.449.580]
        
        Glycogen Storage Disease Type VII [C18.452.648.202.449.600]
        
        Glycogen Storage Disease Type VIII [C18.452.648.202.449.620]

Glycogen Storage Disease Type V Preferred

Concept UI: M0009473
Scope Note: Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
Terms: Glycogen Storage Disease Type V Preferred Term
Term UI T018280
Date01/01/1999
LexicalTag NON
ThesaurusID; Deficiency, Muscle Phosphorylase
Term UI T018284
Date05/31/1988
LexicalTag NON
ThesaurusID UNK (19XX); Glycogen Storage Disease Type 5
Term UI T750080
Date04/27/2009
LexicalTag NON
ThesaurusID; Glycogen Storage Disease V
Term UI T811584
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Glycogenosis 5
Term UI T018281
Date05/31/1988
LexicalTag NON
ThesaurusID; McArdle Disease
Term UI T018282
Date06/15/1984
LexicalTag EPO
ThesaurusID; McArdle Type Glycogen Storage Disease
Term UI T750955
Date05/12/2009
LexicalTag EPO
ThesaurusID; McArdle's Disease
Term UI T018283
Date12/11/1974
LexicalTag EPO
ThesaurusID; Muscle Glycogen Phosphorylase Deficiency
Term UI T750954
Date05/12/2009
LexicalTag NON
ThesaurusID; Muscle Phosphorylase Deficiency
Term UI T018285
Date05/31/1988
LexicalTag NON
ThesaurusID; Myophosphorylase deficiency
Term UI T824108
Date06/19/2012
LexicalTag NON
ThesaurusID; PYGM Deficiency
Term UI T824107
Date06/19/2012
LexicalTag ABX
ThesaurusID; Mcardle Syndrome
Term UI T841529
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Glycogen Storage Disease Type V MeSH Descriptor Data 2024