ORPHA:209013
Acquired amyloid peripheral neuropathy
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired amyloid peripheral neuropathy | |
| fr | Neuropathie périphérique amyloïde acquise | |
| de | Amyloid-Polyneuropathie, erworbene | |
| es | Neuropatía amiloide periférica adquirida | |
| it | Neuropatia periferica amiloide acquisita | |
| nl | Verworven amyloïde perifere neuropathie | |
| pt | Neuropatia amilóide periférica adquirida | |
| pl | Nabyta obwodowa neuropatia amyloidowa | |
| cs | Získaná amyloidová periferní neuropatie | |
| uk | Набута амілоїдна периферична нейропатія | |
| zh | 获得性淀粉样蛋白周围神经病 | |
| tr | Edinsel amiloid periferik nöropati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16179 | E | validated | |
| UMLS | C5680847 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:182086Acquired peripheral neuropathy
rare neurological diseases
Children (2):
4
Genes
0 directOrphanet records no gene directly on this code.
5
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/209013
- This record as JSON: /data/d/209013.json