ORPHA:207006
OBSOLETE: Acquired amyloid myopathy
inactive · referred to ORPHA:206638Acquired skeletal muscle disease
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Acquired skeletal muscle disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Acquired amyloid myopathy | |
| fr | OBSOLETE : Myopathie amyloïde acquise | |
| de | OBSOLET: Amyloidmyopathie, erworbene | |
| es | OBSOLETO: Miopatía amiloide adquirida | |
| it | OBSOLETO: Miopatia amiloide acquisita | |
| nl | OBSOLEET: Verworven amyloïde myopathie | |
| pt | OBSOLETO: Miopatia amilóide adquirida | |
| pl | NIEAKTUALNE: Nabyta miopatia amyloidowa | |
| cs | NEAKTUÁLNÍ: Získaná amyloidová myopatie | |
| uk | ЗАСТАРІЛО: Набута амілоїдна міопатія | |
| zh | 弃用：获得性淀粉样肌病 | |
| tr | Eski adı: Edinsel amiloid miyopati |
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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/207006
- This record as JSON: /data/d/207006.json