Distal 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.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Autosomal dominant distal myopathy | MONDO:0016108 | 15 | |
| Oculopharyngodistal myopathy | MONDO:0025193 | 5 | |
| Miyoshi myopathy | MONDO:0009685 | 3 | |
| GNE myopathy | MONDO:0011603 | ||
| MYH7-related skeletal myopathy | MONDO:0008050 | ||
| Asymptomatic hyperckemia-myalgia-rhabdomyolysis syndrome | MONDO:0975918 | ||
| Distal myopathy with anterior tibial onset | MONDO:0011721 | ||
| Myopathy, distal, 5 | MONDO:0014877 | ADSS1 | |
| Myopathy, distal, 6, adult-onset, autosomal dominant | MONDO:0032853 | ||
| Myopathy, distal, 7, adult-onset, X-linked | MONDO:0024771 | SMPX | |
| Myopathy, distal, infantile-onset | MONDO:0008049 | ||
| Myopathy, distal, with rimmed vacuoles | MONDO:0014945 | ||
| Nebulin-related early-onset distal myopathy | MONDO:0018371 |
Rare disease
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