Glycogen Storage Disease Type V

Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.

Year introduced: 1989(1975)

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.320.565.202.449.560, C18.452.648.202.449.560

MeSH Unique ID: D006012

Entry Terms:

• Deficiency, Muscle Phosphorylase
• Deficiencies, Muscle Phosphorylase
• Muscle Phosphorylase Deficiencies
• Phosphorylase Deficiencies, Muscle
• Phosphorylase Deficiency, Muscle
• Glycogen Storage Disease Type 5
• Glycogen Storage Disease V
• Glycogenosis 5
• Glycogenosis 5s
• McArdle Disease
• Disease, McArdle
• McArdle Type Glycogen Storage Disease
• McArdle's Disease
• Disease, McArdle's
• McArdles Disease
• Muscle Glycogen Phosphorylase Deficiency
• Muscle Phosphorylase Deficiency
• Myophosphorylase deficiency
• deficiencies, Myophosphorylase
• deficiency, Myophosphorylase
• Myophosphorylase deficiencies
• PYGM Deficiency
• Deficiencies, PYGM
• Deficiency, PYGM
• PYGM Deficiencies
• Mcardle Syndrome
• Mcardle Syndromes
• Syndrome, Mcardle
• Syndromes, Mcardle

Previous Indexing:

• Glucosyltransferases/metabolism (1966-1974)
• Glycogenosis (1966-1974)
• Muscular Diseases (1966-1974)

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type V

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type V