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Up to: Hereditary disease · Skeletal muscle disorder
Hereditary skeletal muscle disorder
An instance of muscle tissue disorder that is caused by an inherited genomic modification in an individual.
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Muscular dystrophy 74 trials · 288 incl. sub-types Sub-types →
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Congenital myopathy 8 trials · 75 incl. sub-types Sub-types →
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Congenital diaphragmatic hernia 45 trials Sub-types →
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Myopathy caused by variation in FKRP 0 trials · 8 incl. sub-types Sub-types →
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Hereditary inclusion-body myopathy 1 trial · 6 incl. sub-types Sub-types →
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Poland syndrome 2 trials
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Myopathy caused by variation in FKTN 1 trial · 2 incl. sub-types Sub-types →
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Inherited rippling muscle disease 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in CRPPA 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in GMPPB 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in POMT1 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in POMT2 0 trials · 1 incl. sub-types Sub-types →
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Polyglucosan body myopathy 0 trials · 1 incl. sub-types Sub-types →
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Brody myopathy 0 trials
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FHL1-related myopathy 0 trials Sub-types →
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Myopathy, sarcoplasmic body 0 trials
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Myosclerosis 0 trials
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Potassium-aggravated myotonia 0 trials Sub-types →