ORPHA:94149
Autosomal dominant cerebellar ataxia type IV
Synonyms: ADCA4 · ADCAIV · Autosomal dominant cerebellar ataxia type 4
- 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 IV | ADCA4 · ADCAIV · Autosomal dominant cerebellar ataxia type 4 |
| fr | Ataxie cérébelleuse autosomique dominante type IV | ADCA4 · ADCAIV · Ataxie cérébelleuse autosomique dominante type 4 |
| de | Ataxie, zerebelläre, autosomal-dominante, Typ IV | ADCA4 · ADCAIV · Ataxie, zerebelläre, autosomal-dominante, Typ 4 |
| es | Ataxia cerebelosa autosómica dominante tipo IV | ADCA4 · ADCAIV · Ataxia cerebelosa autosómica dominante tipo 4 |
| it | Atassia cerebellare autosomica dominante, tipo 4 | ADCA4 · ADCAIV · Atassia cerebellare autosomica dominante, tipo IV |
| nl | Autosomaal dominante cerebellaire ataxie type IV | ADCA4 · ADCAIV · Autosomaal dominante cerebellaire ataxie type 4 |
| pt | Ataxia cerebelosa autossómica dominante tipo IV | ADCA4 |
| pl | Autosomalna dominująca ataksja móżdżkowa typu IV | ADCA4 · ADCAIV · Autosomalna dominująca ataksja móżdżkowa typu 4 |
| cs | Autozomálně dominantní cerebelární ataxie, typ 4 | ADCA4 · ADCAIV · Autozomálně dominantní cerebelární ataxie, typ IV |
| uk | Аутосомно-домінантна мозочкова атаксія, тип IV | ADCA4 · ADCAIV · Аутосомно-домінантна мозочкова атаксія типу 4 |
| zh | 常染色体显性遗传性小脑共济失调共济失调IV型 | 常染色体显性遗传性小脑共济失调4型 |
| tr | Otozomal dominant serebellar ataksi tip IV | ADCA4 · ADCAIV · Otozomal baskın serebellar ataksi tip 4 |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019794 | E | validated | |
| UMLS | C5680261 | 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
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/94149
- This record as JSON: /data/d/94149.json