ORPHA:98539
Early-onset ataxia with dementia
- 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 | Early-onset ataxia with dementia | |
| fr | Ataxie à début précoce avec démence | |
| de | Ataxie, früh beginnende, mit Demenz | |
| es | Ataxia de inicio precoz con demencia | |
| it | Atassia ad esordio precoce con demenza | |
| nl | Vroege-aanvang ataxie met dementie | |
| pt | Ataxia de início precoce com demência | |
| pl | Ataksja o wczesnym początku z otępieniem | |
| cs | Časně nastupující ataxie s demencí | |
| uk | Атаксія з раннім початком і деменцією | |
| zh | 早发性共济失调伴痴呆 | |
| tr | Demans ile seyreden erken başlangıçlı ataksi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681725 | 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:98538Ataxia with dementia
rare genetic diseases; rare neurological diseases
Children (1):
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/98539
- This record as JSON: /data/d/98539.json