ORPHA:624259
Non-specific autoimmune cerebellar ataxia with characteristic antibodies
Synonyms: Non-specific autoimmune CA with characteristic antibodies
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-specific autoimmune cerebellar ataxia with characteristic antibodies | Non-specific autoimmune CA with characteristic antibodies |
| fr | Ataxie cérebelleuse auto-immune non-spécifique avec anticorps caractéristiques | AC auto-immune non-spécifique avec anticorps caractéristiques |
| de | Unspezifische autoimmune zerebelläre Ataxie mit charakteristischen Antikörpern | |
| es | Ataxia cerebelosa autoinmune inespecífica con anticuerpos característicos | AC autoinmune inespecífica con anticuerpos característicos |
| it | Atassia cerebellare autoimmune aspecifica con anticorpi caratteristici | AC autoimmune aspecifica con anticorpi caratteristici |
| nl | Aspecifieke auto-immune cerebellaire ataxie met typische antilichamen | Aspecifieke auto-immune CA met typische antilichamen |
| pt | Ataxia cerebelosa autoimune não-específica com anticorpos característicos | CA autoimune não-específica com anticorpos característicos |
| pl | Nieswoista autoimmunologiczna ataksja móżdżkowa z charakterystycznymi przeciwciałami | = en |
| cs | Nespecifická autoimunitní cerebelární ataxie s charakteristickými protilátkami | = en |
| uk | Неспецифічна аутоімунна мозочкова атаксія з характерними антитілами | Неспецифічна аутоімунна ХА з характерними антитілами |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G31.8 | NTBT | attributed | validated |
| MONDO | 0850108 | E | validated | |
| UMLS | C5680404 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:623638Immune-mediated cerebellar ataxia
rare neurological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
3 annotations · validated 2025-08-19| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:6000876 | Anti-Glutamate Receptor delta2 antibody positivity | |
| HP:6000880 | Anti-neurochondrin antibody positivity | |
| HP:6000879 | Anti-regulator of G protein signaling 8 antibody positivity | |
Annotation source: 17008044[PMID]_36437687[PMID]_33782191[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/624259
- This record as JSON: /data/d/624259.json