ORPHA:98693

OBSOLETE: Spinocerebellar ataxia with oculomotor anomaly

inactive · referred to ORPHA:519341Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature

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 Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Spinocerebellar ataxia with oculomotor anomaly
fr	OBSOLETE : Ataxie spinocérébelleuse avec anomalie oculomotrice
de	OBSOLET: Ataxie, spinozerebelläre, mit okulomotorischer Anomalie
es	OBSOLETO: Ataxia espinocerebelosa con anomalía oculomotora
it	OBSOLETO: Atassia spinocerebellare con anomalia oculomotoria
nl	OBSOLEET: Spinocerebellaire ataxie met oculomotorische anomalie
pt	OBSOLETO: Ataxia espinocerebelosa com anomalia oculomotora
pl	NIEAKTUALNE: Ataksja rdzeniowo-mózdzkowa z anomalia okoruchowa
cs	NEAKTUÁLNÍ: Spinocerebelární ataxie s okohybnou anomálií
uk	ЗАСТАРІЛО: Спіноцеребеллярна атаксія з окоруховою аномалією
zh	弃用：脊髓小脑性共济失调与动眼神经异常
tr	Eski adı: Okülomotor anomali ile seyreden 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/98693
This record as JSON: /data/d/98693.json