raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98070

OBSOLETE: Autosomal dominant spinocerebellar ataxia due to repeat expansions that do not encode polyglutamine

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Autosomal dominant spinocerebellar ataxia due to repeat expansions that do not encode polyglutamine
frOBSOLETE : Ataxie spinocérébelleuse autosomique dominante due à des expansions non codantes pour la polyglutamine
deOBSOLET: Ataxie, spinozerebelläre, bei Repeat-Expansionen, die nicht Polyglutamin betreffen
esOBSOLETO: Ataxia espinocerebelosa autosómica dominante por expansiones repetidas que no codifican para poliglutamina
itOBSOLETO: Atassia spinocerebellare da ripetute espansioni che non codificano per poliglutamine
nlOBSOLEET: Autosomaal dominante spinocerebellaire ataxie als gevolg van herhaalde expansies die geen polyglutamine coderen
ptOBSOLETO: Ataxia espinocerebelosa autossómica dominante por expansões repetitivas que não codificam poliglutamina
plNIEAKTUALNE: Autosomalna dominujaca ataksja rdzeniowo-mózdzkowa z powodu ekspansji powtórzen, które nie koduja poliglutaminy
csNEAKTUÁLNÍ: Autozomálně dominantní spinocerebelární ataxie způsobená expanzí repetitivních sekvencí nekódujících polyglutamin
ukЗАСТАРІЛО: Аутосомно-домінантна спіноцеребеллярна атаксія внаслідок повторних експансій, які не кодують поліглутамін.
zh弃用:不编码多聚谷氨酰胺重复扩张致常染色体显性遗传脊髓小脑性共济失调
trEski adı: Poliglutamini kodlamayan tekrarlayan genişlemelere bağlı otozomal dominant spinoserebellar ataksi
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No 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