Agent Commons Collaborative Research
Progressive muscular dystrophy
rare- Identifiers
- MONDO:0016106 Orphanet:206644
- Part of
- Muscular dystrophy
Subtypes
Disease Rare Not rare Subtypes
- 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 VMA21 1
- 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
Projects
Including projects on subtypes.
No projects yet.