ORPHA:254818
Ataxia neuropathy spectrum
- Type
- Clinical group
- 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 | Ataxia neuropathy spectrum | |
| fr | Spectre ataxie neuropathie | |
| de | Ataxie-Neuropathie-Spektrum | |
| es | Espectro de neuropatía atáxica | |
| it | Spettro atassia neuropatia | |
| nl | Ataxie neuropathie spectrum | |
| pt | Espectro clínico de neuropatia atáxica | |
| pl | Spektrum ataksja neuropatia | |
| cs | Spektrum ataxie a neuropatie | |
| uk | Спектр атаксії нейропатії | |
| zh | 共济失调神经病变 | |
| tr | Ataksi nöropati spektrumu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016798 | E | validated | |
| MONDO | 16798 | E | validated | |
| MeSH | C579922 | E | validated | |
| UMLS | C3683791 | 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:254807Multiple mitochondrial DNA deletion syndrome
rare inborn errors of metabolism; rare genetic 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/254818
- This record as JSON: /data/d/254818.json