ORPHA:54238
Myotonic dystrophy type 3
inactive · moved to ORPHA:52430Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Myotonic dystrophy type 3 | |
| fr | Dystrophie myotonique type 3 | |
| de | Myotone Dystrophie Typ 3 | |
| es | Distrofia miotónica tipo 3 | |
| it | Distrofia miotonica, tipo 3 | |
| nl | Myotonische dystrofie type 3 | |
| pt | Distrofia miotónica tipo 3 | |
| pl | Dystrofia miotoniczna typu 3 | |
| cs | Myotonická dystrofie, typ 3 | |
| uk | Міотонічна дистрофія, тип 3 | |
| zh | 强直性肌营养不良3型 | |
| tr | Miyotonik distrofi tip 3 |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/54238
- This record as JSON: /data/d/54238.json