Distal myopathy
MONDO:0018949Distal myopathy refers to a group of muscle diseases which share the clinical pattern of predominant weakness and atrophy beginning in the feet and/or hands.
Also known as: distal muscular dystrophy, distal myopathy, Miyoshi muscular dystrophy
8 clinical trials for this condition and its sub-types, 1 tagged with Distal myopathy itself.
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Sub-types of Distal myopathy
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Miyoshi myopathy 1 trial · 2 incl. sub-types
3 sub-types
- Miyoshi muscular dystrophy 3 1 trial
- Miyoshi muscular dystrophy 1 0 trials
- Miyoshi muscular dystrophy 2 0 trials
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Myopathy, distal, 5 1 trial
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MYH7-related skeletal myopathy 0 trials
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Autosomal dominant distal myopathy 0 trials
15 sub-types
- Finnish upper limb-onset distal myopathy 0 trials
- KLHL9-related early-onset distal myopathy 0 trials
- TARDBP-related predominantly upper-limb distal myopathy 0 trials
- Adult-onset distal myopathy due to VCP mutation 0 trials
- Asymetric thumb-handgrip weakness-distal myopathy 0 trials
- Calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathy 0 trials
- Distal myopathy with posterior leg and anterior hand involvement 0 trials
- Distal myopathy with vocal cord weakness 0 trials
- Distal myopathy, Tateyama type 0 trials
- Distal myopathy, Welander type 0 trials
- Myofibrillar myopathy 2 0 trials
- Myofibrillar myopathy 3 0 trials
- Myofibrillar myopathy 4 0 trials
- Myopathy, myofibrillar, 9, with early respiratory failure 0 trials
- Tibial muscular dystrophy 0 trials
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Myopathy, distal, infantile-onset 0 trials
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Oculopharyngodistal myopathy 0 trials
5 sub-types
- Oculopharyngodistal myopathy 1 0 trials
- Oculopharyngodistal myopathy 2 0 trials
- Oculopharyngodistal myopathy 3 0 trials
- Oculopharyngodistal myopathy 4 0 trials
- Oculopharyngodistal myopathy 5 0 trials