ORPHA:207028
Cerebellar ataxia with peripheral neuropathy
- Type
- Category
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cerebellar ataxia with peripheral neuropathy | |
| fr | Ataxie cerebelleuse avec neuropathie périphérique | |
| de | Kleinhirnataxie mit peripherer Neuropathie | |
| es | Ataxia cerebelosa con neuropatía periférica | |
| it | Atassia cerebellare con neuropatia periferica | |
| nl | Cerebellaire ataxie met perifere neuropathie | |
| pt | Ataxia cerebelosa com neuropatia periférica | |
| pl | Ataksja móżdżkowa z neuropatią obwodową | |
| cs | Cerebelární ataxie s periferní neuropatií | |
| uk | Мозочкова атаксія з периферичною нейропатією | |
| zh | 小脑共济失调伴周围神经病的 | |
| tr | Periferik nöropati ile seyreden serebellar ataksi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G60.2 | E | specific | validated |
| MONDO | 16136 | E | validated | |
| UMLS | C5680815 | 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:207025Rare hereditary neurologic disease with peripheral neuropathy
rare genetic diseases; rare neurological diseases
Children (7):
- ORPHA:504476Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
- ORPHA:694922Childhood-onset stress-induced neurodegenerative ataxia-seizure syndrome
- ORPHA:48431Congenital cataracts-facial dysmorphism-neuropathy syndrome
- ORPHA:95Friedreich ataxia
- ORPHA:559Marinesco-Sjögren syndrome
- ORPHA:715623Motor incoordination-myopathy-respiratory insufficiency-progressive cerebellar atrophy syndrome
- ORPHA:589522Spinocerebellar ataxia type 46
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
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/207028
- This record as JSON: /data/d/207028.json