raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98770

Spinocerebellar ataxia type 16

inactive · moved to ORPHA:98769Spinocerebellar ataxia type 15/16

Synonyms: SCA16

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Spinocerebellar ataxia type 15/16

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enSpinocerebellar ataxia type 16SCA16
frAtaxie spinocérébelleuse type 16= en
deAtaxie, spinozerebelläre, Typ 16= en
esAtaxia espinocerebelosa tipo 16= en
itAtassia spinocerebellare, tipo 16= en
nlSpinocerebellaire ataxie type 16= en
ptAtaxia espinocerebelosa tipo 16= en
plAtaksja rdzeniowo-móżdżkowa typu 16= en
csSpinocerebelární ataxie, typ 16= en
ukСпіноцеребеллярна атаксія, тип 16= en
zh脊髓小脑共济失调16型= en
trSpinoserebellar ataksi tip 16= en
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.

7

Sources for this card