raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:623638

Immune-mediated cerebellar ataxia

Synonyms: Autoimmune cerebellitis · IMCA

Type
Clinical group
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enImmune-mediated cerebellar ataxiaAutoimmune cerebellitis · IMCA
frAtaxie cérébelleuse immuno-médiéeAtaxie cérébelleuse auto-immune · Cérébellite auto-immune
deImmune-vermittelte zerebelläre AtaxieAutoimmune Zerebellitis · IMCA · Kleinhirnentzündung, autoimmune
esAtaxia cerebelosa inmunomediadaCerebelitis autoinmune
itAtassia cerebellare immuno-mediataCerebellite autoimmune · IMCA
nlImmuungemedieerde cerebellaire ataxieAuto-immune cerebellitis · IMCA
ptAtaxia cerebelosa imunomediadaCerebelite autoimune · IMCA
plAtaksja móżdżkowa o podłożu immunologicznym= en
csAutoimunitní cerebelární ataxie= en
ukІмуноопосередкована мозочкова атаксіяАутоімунний церебелліт · IMCA
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0859692Evalidated
UMLSC5680410Evalidated

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 (2):

Children (4):

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