raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:624268

Non-specific autoimmune cerebellar ataxia without characteristic antibodies

Synonyms: Non-specific autoimmune CA without characteristic antibodies · PACA · Primary Autoimmune Cerebellar Ataxia

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
All ages
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enNon-specific autoimmune cerebellar ataxia without characteristic antibodiesNon-specific autoimmune CA without characteristic antibodies · PACA · Primary Autoimmune Cerebellar Ataxia
frAtaxie cérébelleuse auto-immune non-spécifique sans anticorps caractéristiquesAtaxie cérébelleuse auto-immune primitive · CA auto-immune non-spécifique sans anticorps caractéristiques
deUnspezifische autoimmune zerebelläre Ataxie ohne charakteristische AntikörperPACA · Primäre autoimmune zerebelläre Ataxie
esAtaxia cerebelosa autoinmune inespecífica sin anticuerpos característicosAC autoinmune inespecífica sin anticuerpos característicos · Ataxia cerebelosa autoinmune primaria · PACA
itAtassia cerebellare autoimmune aspecifica senza anticorpi caratteristiciAC autoimmune aspecifica senza anticorpi caratteristici · ACAP · Atassia cerebellare autoimmune primitiva
nlAspecifieke auto-immune cerebellaire ataxie zonder typische antilichamenAspecifieke auto-immune CA zonder typische antilichamen · PACA · Primaire auto-immune cerebellaire ataxie
ptAtaxia cerebelosa autoimune não-específica sem anticorpos característicosAtaxia cerebelosa autoimune primária · PACA
plNieswoista autoimmunologiczna ataksja móżdżkowa bez charakterystycznych przeciwciał= en
csNespecifická autoimunitní cerebelární ataxie bez charakteristických protilátek= en
ukНеспецифічна аутоімунна мозочкова атаксія без характерних антитілНеспецифічний аутоімунний ХА без характерних антитіл · PACA · Первинна аутоімунна мозочкова атаксія
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10G31.8NTBTattributedvalidated
MONDO0850109Evalidated
UMLSC5576703Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyValidatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

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

7

Sources for this card