ORPHA:98073

OBSOLETE: Unclassified autosomal dominant spinocerebellar ataxia

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: Unclassified autosomal dominant spinocerebellar ataxia
fr	OBSOLETE : Ataxie spinocérébelleuse autosomique dominante non classifiée
de	OBSOLET: Ataxie, spinozerebelläre, autosomal-dominante, durch sonstige Ursachen
es	OBSOLETO: Ataxia espinocerebelosa autosómica dominante no clasificada
it	OBSOLETO: Atassia spinocerebellare, autosomica dominante, dovuta ad altre cause
nl	OBSOLEET: Niet-geclassificeerde autosomaal dominante spinocerebellaire ataxie
pt	OBSOLETO: Ataxia espinocerebelosa autossómica dominante devida a outras causas
pl	NIEAKTUALNE: Niesklasyfikowana autosomalna dominujaca ataksja rdzeniowo-mózdzkowa
cs	NEAKTUÁLNÍ: Neklasifikované autozomálně dominantní spinocerebelární ataxie
uk	ЗАСТАРІЛО: Некласифікована аутосомно-домінантна спіноцеребеллярна атаксія
zh	弃用：未分类常染色体显性遗传脊髓小脑性共济失调
tr	Eski adı: Sınıflandırılmamış 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/98073
This record as JSON: /data/d/98073.json