ORPHA:101107
Spinocerebellar ataxia type 22
inactive · moved to ORPHA:98772Spinocerebellar ataxia type 19/22
Synonyms: SCA22
- 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 19/22
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spinocerebellar ataxia type 22 | SCA22 |
| fr | Ataxie spinocérébelleuse type 22 | = en |
| de | Ataxie, spinozerebelläre, Typ 22 | = en |
| es | Ataxia espinocerebolosa tipo 22 | = en |
| it | Atassia spinocerebellare, tipo 22 | = en |
| nl | Spinocerebellaire ataxie type 22 | = en |
| pt | Ataxia espinocerebelosa tipo 22 | = en |
| pl | Ataksja rdzeniowo-móżdżkowa typu 22 | = en |
| cs | Spinocerebelární ataxie, typ 22 | = en |
| uk | Спіноцеребеллярна атаксія, тип 22 | = en |
| zh | 脊髓小脑共济失调22型 | = en |
| tr | Spinoserebellar ataksi tip 22 | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C542540 | E | validated | |
| UMLS | C2746067 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/101107
- This record as JSON: /data/d/101107.json