ORPHA:206613
Infectious disease with 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infectious disease with peripheral neuropathy | |
| fr | Maladie infectieuse avec neuropathie périphérique | |
| de | Infektionskrankheit mit peripherer Neuropathie | |
| es | Enfermedad infecciosa con neuropatía periférica | |
| it | Malattia infettiva con neuropatia periferica | |
| nl | Infectieuze ziekte met perifere neuropathie | |
| pt | Doença infeciosa com neuropatia periférica | |
| pl | Choroba zakaźna z neuropatią obwodową | |
| cs | Infekční nemoci s periferní neuropatií | |
| uk | Інфекційне захворювання з периферичною нейропатією | |
| zh | 伴周围神经病的感染性疾病 | |
| tr | Periferik nöropati ile seyreden bulaşıcı hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16104 | E | validated | |
| UMLS | C1278821 | 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:182086Acquired peripheral neuropathy
rare neurological diseases
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/206613
- This record as JSON: /data/d/206613.json