ORPHA:206644
Progressive muscular dystrophy
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Progressive muscular dystrophy | |
| fr | Dystrophie musculaire progressive | |
| de | Muskeldystrophie, progressive | |
| es | Distrofia muscular progresiva | |
| it | Distrofia muscolare progressiva | |
| nl | Progressieve spierdystrofie | |
| pt | Distrofia muscular progressiva | |
| pl | Postępująca dystrofia mięśniowa | |
| cs | Progresivní svalová dystrofie | |
| uk | Прогресуюча мязова дистрофія | |
| zh | 进行性肌营养不良症 | |
| tr | İlerleyici kas distrofisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016106 | E | validated | |
| MONDO | 16106 | E | validated | |
| UMLS | C4551827 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98473Muscular dystrophy
rare genetic diseases; rare neurological diseases
Children (17):
- ORPHA:610Bethlem muscular dystrophy
- ORPHA:466921Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome
- ORPHA:45358Congenital fibrosis of extraocular muscles
- ORPHA:262Duchenne and Becker muscular dystrophy
- ORPHA:261Emery-Dreifuss muscular dystrophy
- ORPHA:257Epidermolysis bullosa simplex with muscular dystrophy
- ORPHA:269Facioscapulohumeral dystrophy
- ORPHA:178464Hereditary myopathy with early respiratory failure
- ORPHA:431263Late-onset scapuloperoneal muscular dystrophy with hyaline bodies
- ORPHA:263Limb-girdle muscular dystrophy
- ORPHA:206647Myotonic dystrophy
- ORPHA:270Oculopharyngeal muscular dystrophy
- ORPHA:98897Oculopharyngodistal myopathy
- ORPHA:447977Progressive scapulohumeroperoneal distal myopathy
- ORPHA:800Schwartz-Jampel syndrome
- ORPHA:25980X-linked myopathy with excessive autophagy
- ORPHA:178461X-linked myopathy with postural muscle atrophy
Codes that Orphanet moved or referred to this one:
- ORPHA:238755OBSOLETE: Autosomal dominant limb-girdle muscular dystrophy type 1H referred to · inactive
- ORPHA:466801OBSOLETE: LIMS2-related myopathy referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/206644
- This record as JSON: /data/d/206644.json