ORPHA:316226
Spastic ataxia
Synonyms: SPAX
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spastic ataxia | SPAX |
| fr | Ataxie spastique | = en |
| de | Spastische Ataxie | = en |
| es | Ataxia espástica | = en |
| it | Atassia spastica | = en |
| nl | Spastische ataxie | = en |
| pt | Ataxia espástica | = en |
| pl | Ataksja spastyczna | = en |
| cs | Spastická ataxie | = en |
| uk | Спастична атаксія | = en |
| zh | 痉挛性共济失调 | = en |
| tr | Spastik ataksi | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017845 | E | validated | |
| MONDO | 17845 | E | validated | |
| MeSH | C564815 | E | validated | |
| UMLS | C1849156 | 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:183518Hereditary ataxia
rare genetic diseases; 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/316226
- This record as JSON: /data/d/316226.json