ORPHA:247765
X-linked cerebellar ataxia
- Type
- Category
- Group
- Group of disorders
- Inheritance
- X-linked dominant, X-linked recessive
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | X-linked cerebellar ataxia | |
| fr | Ataxie cérébelleuse liée à l'X | |
| de | Zerebelläre Ataxie, X-chromosomale | |
| es | Ataxia cerebelosa ligada al cromosoma X | |
| it | Atassia cerebellare legata all'X | |
| nl | X-gebonden cerebellaire ataxie | |
| pt | Ataxia cerebelosa ligada ao X | |
| pl | Ataksja móżdżkowa sprzężona z X | |
| cs | X-vázaná spinocerebelární ataxie | |
| uk | Х-зчеплена мозочкова атаксія | |
| zh | x连锁遗传小脑性共济失调 | |
| tr | X'e bağlı serebellar ataksi |
2
Cross-references
qualifier = Orphanet mapping relationE 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):
- ORPHA:183518Hereditary ataxia
rare genetic diseases; rare neurological diseases
Children (10):
- ORPHA:1188Ataxia-deafness-intellectual disability syndrome
- ORPHA:85278Christianson syndrome
- ORPHA:93256Fragile X-associated tremor/ataxia syndrome
- ORPHA:1187Lethal ataxia with deafness and optic atrophy
- ORPHA:85338X-linked intellectual disability-ataxia-apraxia syndrome
- ORPHA:314978X-linked non progressive cerebellar ataxia
- ORPHA:1175X-linked progressive cerebellar ataxia
- ORPHA:2802X-linked sideroblastic anemia and spinocerebellar ataxia
- ORPHA:85297X-linked spinocerebellar ataxia type 3
- ORPHA:85292X-linked spinocerebellar ataxia type 4
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/247765
- This record as JSON: /data/d/247765.json