ORPHA:98069

OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a channelopathy

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

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a channelopathy
fr	OBSOLETE : Ataxie spinocérébelleuse autosomique dominante due à une canalopathie
de	OBSOLET: Ataxie, spinozerebelläre, bei Ionenkanalkrankheit
es	OBSOLETO: Ataxia espinocerebelosa autosómica dominante por canalopatía
it	OBSOLETO: Atassia spinocerebellare da canalopatia
nl	OBSOLEET: Autosomaal dominante spinocerebellaire ataxie als gevolg van een kanalopathie
pt	OBSOLETO: Ataxia espinhocerebelosa autossómica dominante por canalopatia
pl	NIEAKTUALNE: Autosomalna dominujaca ataksja rdzeniowo-mózdzkowa z powodu kanalopatii
cs	NEAKTUÁLNÍ: Autozomálně dominantní spinocerebelární ataxie způsobená kanálopatií
uk	ЗАСТАРІЛО: Аутосомно-домінантна спіноцеребеллярна атаксія внаслідок каналопатії
zh	弃用：离子通道病致常染色体显性脊髓小脑共济失调遗传病
tr	Eski adı: Kanalopatiye bağlı otozomal dominant spinoserebellar ataksi

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/98069
This record as JSON: /data/d/98069.json