ORPHA:208508
Autosomal dominant cerebellar ataxia type II
Synonyms: ADCA2 · ADCAII · Autosomal dominant cerebellar ataxia type 2
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Autosomal dominant
- 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 | Autosomal dominant cerebellar ataxia type II | ADCA2 · ADCAII · Autosomal dominant cerebellar ataxia type 2 |
| fr | Ataxie cérébelleuse autosomique dominante type II | ADCA2 · ADCAII · Ataxie cérébelleuse autosomique dominante type 2 |
| de | Ataxie, zerebelläre, autosomal-dominante, Typ II | ADCA2 · ADCAII · Ataxie, zerebelläre, autosomal-dominante, Typ 2 |
| es | Ataxia cerebelosa autosómica dominante tipo II | ADCA2 · ADCAII · Ataxia cerebelosa autosómica dominante tipo 2 |
| it | Atassia cerebellare, autosomica dominante, tipo 2 | ADCA2 · ADCAII · Atassia cerebellare, autosomica dominante, tipo II |
| nl | Autosomaal dominante cerebellaire ataxie type II | ADCA2 · ADCAII · Autosomaal dominante cerebellaire ataxie type 2 |
| pt | Ataxia cerebelosa autossómica dominante tipo II | ADCA2 |
| pl | Autosomalna dominująca ataksja móżdżkowa typu II | ADCA2 · ADCAII · Autosomalna dominująca ataksja móżdżkowa typu 2 |
| cs | Autozomálně dominantní cerebelární ataxie, typ 2 | ADCA2 · ADCAII · Autozomálně dominantní cerebelární ataxie, typ II |
| uk | Аутосомно-домінантна мозочкова атаксія, тип II | ADCA2 · ADCAII · Аутосомно-домінантна мозочкова атаксія типу 2 |
| zh | 常染色体显性遗传小脑型共济失调Ⅱ型 | 常染色体显性遗传小脑型共济失调2型 |
| tr | Otozomal dominant serebellar ataksi tip II | ADCA2 · ADCAII · Otozomal baskın serebellar ataksi tip 2 |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16163 | E | validated | |
| UMLS | C5848204 | 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:99Autosomal dominant cerebellar ataxia
rare genetic diseases; rare neurological diseases
Children (1):
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Genes
0 directOrphanet records no gene directly on this code.
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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/208508
- This record as JSON: /data/d/208508.json