ORPHA:98068
OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a polyglutamine anomaly
inactive · referred to ORPHA:99Autosomal dominant cerebellar ataxia
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Autosomal dominant cerebellar ataxia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a polyglutamine anomaly | |
| fr | OBSOLETE : Ataxie spinocérébelleuse autosomique dominante due à une anomalie de la polyglutamine | |
| de | OBSOLET: Ataxie, spinozerebelläre, bei Polyglutamin-Anomalie | |
| es | OBSOLETO: Ataxia espinocerebelosa autosómica dominante por una anomalía de la poliglutamina | |
| it | OBSOLETO: Atassia spinocerebellare da anomalia delle poliglutamine | |
| nl | OBSOLEET: Autosomaal dominante spinocerebellaire ataxie als gevolg van een polyglutamineanomalie | |
| pt | OBSOLETO: Ataxia espinocerebelosa autossómica dominante por anomalia de poliglutamina | |
| pl | NIEAKTUALNE: Autosomalna dominujaca ataksja rdzeniowo-mózdzkowa z powodu anomalii poliglutaminy | |
| cs | NEAKTUÁLNÍ: Autozomálně dominantní spinocerebelární ataxie způsobená anomálií polyglutaminu | |
| uk | ЗАСТАРІЛО: Аутосомно-домінантна спіноцеребелярна атаксія внаслідок поліглутамінової аномалії | |
| zh | 弃用：多谷氨酰胺异常致常染色体显性失调遗传脊髓小脑性共济失调 | |
| tr | Eski adı: Poliglutamin anomalisine bağlı otozomal dominant spinoserebellar ataksi |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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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/98068
- This record as JSON: /data/d/98068.json