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Results 1 - 8 of 8 for Myalgia
  1. Carnitine palmitoyltransferase II deficiency 
    ... is characterized by recurrent episodes of muscle pain (myalgia) and occasional weakness that is associated with the ... to be red or brown (myoglobinuria). Episodes of myalgia and rhabdomyolysis may be triggered by exercise, stress, ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  2. Glycogen storage disease type 0 
    ... disease 0 presenting recurrent syncope with weakness and myalgia. Neuromuscul Disord. 2012 Feb;22(2):162-5. ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  3. GYS1 gene 
    ... disease 0 presenting recurrent syncope with weakness and myalgia. Neuromuscul Disord. 2012 Feb;22(2):162-5. ...
    https://medlineplus.gov/genetics/gene/gys1 - Genetics
  4. Central core disease 
    ... walk independently. Affected individuals may experience muscle pain (myalgia) or extreme fatigue in response to physical activity ( ...
    https://medlineplus.gov/genetics/condition/central-core-disease - Genetics
  5. Multiminicore disease 
    ... Individuals with this form may experience muscle pain (myalgia) or extreme fatigue in response to physical activity ( ...
    https://medlineplus.gov/genetics/condition/multiminicore-disease - Genetics
  6. Mitochondrial complex I deficiency 
    ... may have low muscle tone (hypotonia), muscle pain (myalgia), and extreme fatigue in response to physical activity ( ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  7. Adenosine monophosphate deaminase deficiency 
    ... do experience symptoms typically have fatigue, muscle pain (myalgia), or cramps after exercise or prolonged physical activity ( ...
    https://medlineplus.gov/...nosine-monophosphate-deaminase-deficiency - Genetics
  8. Myofibrillar myopathy 
    ... include a weakened heart muscle (cardiomyopathy), muscle pain (myalgia), loss of sensation and weakness in the limbs ( ...
    https://medlineplus.gov/genetics/condition/myofibrillar-myopathy - Genetics