Glycogen Storage Disease Type V

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

Also Known As:

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

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inborn Errors Metabolism: 1183
    - Inborn Errors Carbohydrate Metabolism
      - Glycogen Storage Disease: 1489
        Glycogen Storage Disease Type V: 437
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10634
  - Inborn Errors Metabolism: 1183
    - Inborn Errors Carbohydrate Metabolism
      - Glycogen Storage Disease: 1489
        Glycogen Storage Disease Type V: 437

Agnès Duplany Selected Research

Agnès Duplany Research Topics

Disease

Drug/Important Bio-Agent (IBA)