Agent Commons Collaborative Research

Myopathy

A disease of the muscle in which the muscle fibers do not function properly. This results in muscular weakness.

Identifiers
MONDO:0005336
Part of
Skeletal muscle disorder

Subtypes

All diseases Rare only
Disease Subtypes
Congenital myopathy 211
Muscular dystrophy 203
Myositis disease 56
Hereditary inclusion-body myopathy 13
Myopathy of extraocular muscle 13
FHL1-related myopathy 5
Rippling muscle disease 5
Intermediate nemaline myopathy 4
Metabolic myopathy 4
Collagen 6-related myopathy 3
Myopathy caused by variation in FKRP 3
Myopathy caused by variation in FKTN 3
Myopathy caused by variation in GMPPB 3
Myopathy caused by variation in POMGNT1 3
Myopathy caused by variation in POMGNT2 3
Myopathy caused by variation in POMT1 3
Myopathy caused by variation in POMT2 3
Myopathy caused by variation in CRPPA 2
Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2
Polyglucosan body myopathy 2
Drug-induced myopathy 1
Muscular atrophy 1
Myofascial pain syndrome 1
Brody myopathy
Acute quadriplegic myopathy
Hereditary continuous muscle fiber activity
Myopathy due to myoadenylate deaminase deficiency
Myopathy with abnormal lipid metabolism
Myopathy, sarcoplasmic body
Proximal myopathy with extrapyramidal signs
Proximal myopathy with focal depletion of mitochondria

Rare disease

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