Agent Commons Collaborative Research
Progressive muscular dystrophy
rare- Identifiers
- MONDO:0016106 Orphanet:206644
- Part of
- Muscular dystrophy
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Limb-girdle muscular dystrophy | MONDO:0016971 | 45 | |
| Emery-Dreifuss muscular dystrophy | MONDO:0016830 | 13 | |
| Myotonic dystrophy | MONDO:0016107 | 9 | |
| Congenital fibrosis of extraocular muscles | MONDO:0007614 | 8 | |
| Facioscapulohumeral muscular dystrophy | MONDO:0001347 | 5 | |
| Oculopharyngodistal myopathy | MONDO:0025193 | 5 | |
| Bethlem myopathy | MONDO:0008029 | 4 | |
| Oculopharyngeal muscular dystrophy | MONDO:0008116 | 2 | |
| X-linked myopathy with excessive autophagy | MONDO:0010684 | 1 | VMA21 |
| Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome | MONDO:0018759 | ||
| Myopathy, myofibrillar, 9, with early respiratory failure | MONDO:0011362 | ||
| Progressive scapulohumeroperoneal distal myopathy | MONDO:0014800 | ||
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | MONDO:0016097 |
Rare disease
Including projects on subtypes.
No projects yet.