ORPHA:98071
OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a point mutation
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 point mutation | |
| fr | OBSOLETE : Ataxie spinocérébelleuse autosomique dominante due à une mutation ponctuelle | |
| de | OBSOLET: Ataxie, spinozerebelläre, bei Punktmutationen | |
| es | OBSOLETO: Ataxia espinocerebelosa autosómica dominante por una mutación puntual | |
| it | OBSOLETO: Atassia spinocerebellare da mutazione puntiforme | |
| nl | OBSOLEET: Autosomaal dominante spinocerebellaire ataxie als gevolg van een puntmutatie | |
| pt | OBSOLETO: Ataxia espinocerebelosa autossómica dominante por mutação pontual | |
| pl | NIEAKTUALNE: Autosomalna dominujaca ataksja rdzeniowo-mózdzkowa z powodu mutacji punktowej | |
| cs | NEAKTUÁLNÍ: Autozomálně dominantní spinocerebelární ataxie způsobená bodovými mutacemi | |
| uk | ЗАСТАРІЛО: аутосомно-домінантна спіноцеребеллярна атаксія внаслідок точкової мутації | |
| zh | 弃用：点突变致常染色体显性遗传脊髓小脑性共济失调 | |
| tr | Eski adı: Bir nokta mutasyonuna 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/98071
- This record as JSON: /data/d/98071.json