Skeletal muscle disorder

Part of

Sub-types of Skeletal muscle disorder

• Myopathy 16 trials · 990 incl. sub-types
  32 sub-types

  • Myositis disease 105 trials · 298 incl. sub-types Sub-types →
  • Muscular dystrophy 74 trials · 290 incl. sub-types Sub-types →
  • Myofascial pain syndrome 157 trials · 228 incl. sub-types Sub-types →
  • Muscular atrophy 97 trials Sub-types →
  • Congenital myopathy 8 trials · 75 incl. sub-types Sub-types →
  • Acute quadriplegic myopathy 14 trials
  • Myopathy caused by variation in FKRP 0 trials · 8 incl. sub-types Sub-types →
  • Hereditary inclusion-body myopathy 1 trial · 6 incl. sub-types Sub-types →
  • Myopathy of extraocular muscle 1 trial · 5 incl. sub-types Sub-types →
  • Drug-induced myopathy 2 trials Sub-types →
  • Myopathy caused by variation in FKTN 1 trial · 2 incl. sub-types Sub-types →
  • Collagen 6-related myopathy 1 trial Sub-types →
  • Metabolic myopathy 1 trial Sub-types →
  • Myopathy caused by variation in CRPPA 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in GMPPB 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in POMT1 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in POMT2 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy due to myoadenylate deaminase deficiency 1 trial
  • Polyglucosan body myopathy 0 trials · 1 incl. sub-types Sub-types →
  • Rippling muscle disease 0 trials · 1 incl. sub-types Sub-types →
  • Brody myopathy 0 trials
  • FHL1-related myopathy 0 trials Sub-types →
  • Hereditary continuous muscle fiber activity 0 trials
  • Intermediate nemaline myopathy 0 trials Sub-types →
  • Myopathy caused by variation in POMGNT2 0 trials Sub-types →
  • Myopathy with abnormal lipid metabolism 0 trials
  • Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 0 trials
  • Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2 0 trials
  • Myopathy, sarcoplasmic body 0 trials
  • Proximal myopathy with extrapyramidal signs 0 trials
  • Proximal myopathy with focal depletion of mitochondria 0 trials
• Hereditary skeletal muscle disorder 1 trial · 406 incl. sub-types
  33 sub-types

  • Muscular dystrophy 74 trials · 290 incl. sub-types Sub-types →
  • Congenital myopathy 8 trials · 75 incl. sub-types Sub-types →
  • Congenital diaphragmatic hernia 45 trials Sub-types →
  • Myopathy caused by variation in FKRP 0 trials · 8 incl. sub-types Sub-types →
  • Hereditary inclusion-body myopathy 1 trial · 6 incl. sub-types Sub-types →
  • Poland syndrome 2 trials
  • Myopathy caused by variation in FKTN 1 trial · 2 incl. sub-types Sub-types →
  • Inherited rippling muscle disease 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in CRPPA 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in GMPPB 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in POMT1 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy caused by variation in POMT2 0 trials · 1 incl. sub-types Sub-types →
  • Myopathy due to myoadenylate deaminase deficiency 1 trial
  • Paramyotonia congenita of Von Eulenburg 1 trial
  • Polyglucosan body myopathy 0 trials · 1 incl. sub-types Sub-types →
  • ACTN2-related cardiac and skeletal myopathy 0 trials Sub-types →
  • Brody myopathy 0 trials
  • FHL1-related myopathy 0 trials Sub-types →
  • Wieacker-Wolff syndrome (spectrum) 0 trials Sub-types →
  • Hereditary continuous muscle fiber activity 0 trials
  • Hereditary myopathy with lactic acidosis due to ISCU deficiency 0 trials
  • Metabolic myopathy due to lactate transporter defect 0 trials
  • Myopathy caused by variation in POMGNT2 0 trials Sub-types →
  • Myopathy due to calsequestrin and SERCA1 protein overload 0 trials
  • Myopathy with abnormal lipid metabolism 0 trials
  • Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 0 trials
  • Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2 0 trials
  • Myopathy, sarcoplasmic body 0 trials
  • Myosclerosis 0 trials
  • Potassium-aggravated myotonia 0 trials Sub-types →
  • Proximal myopathy with extrapyramidal signs 0 trials
  • Proximal myopathy with focal depletion of mitochondria 0 trials
• Rotator cuff syndrome 272 trials
• Acquired skeletal muscle disease 0 trials · 166 incl. sub-types
  5 sub-types

  • Acquired idiopathic inflammatory myopathy 67 trials · 159 incl. sub-types Sub-types →
  • Idiopathic camptocormia 7 trials
  • Acquired rippling muscle disease 0 trials Sub-types →
  • Idiopathic dropped head syndrome 0 trials
  • Macrophagic myofasciitis 0 trials
• Diaphragm disorder 27 trials · 91 incl. sub-types
  5 sub-types

  • Congenital diaphragmatic hernia 45 trials Sub-types →
  • Respiratory paralysis 20 trials
  • Diaphragmatic eventration 3 trials
  • Diaphragmatic malformation 1 trial
  • Diaphragmitis 0 trials
• Myotonic syndrome 11 trials · 61 incl. sub-types
  5 sub-types

  • Myotonic dystrophy 56 trials · 57 incl. sub-types Sub-types →
  • Nondystrophic myotonia 4 trials
  • Laryngospasm, severe neonatal episodic 1 trial
  • Paramyotonia congenita of Von Eulenburg 1 trial
  • Potassium-aggravated myotonia 0 trials Sub-types →
• Anismus 12 trials
• Anterior compartment of tibia syndrome 1 trial
• Cyprus facial-neuromusculoskeletal syndrome 0 trials
• Tel Hashomer camptodactyly syndrome 0 trials
• Volkmann contracture 0 trials
• Muscular dystrophy-white matter spongiosis syndrome 0 trials
• Skeletal muscle neoplasm 0 trials
  2 sub-types

  • Benign skeletal muscle neoplasm 0 trials
  • Skeletal muscle cancer 0 trials