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Glycogen Storage Disease Type V MeSH Descriptor Data 2023


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
Glycogen Storage Disease Type V Preferred
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