ORPHA:182079
ARX-related epileptic encephalopathy
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | ARX-related epileptic encephalopathy | |
| fr | Encéphalopathie épileptique liée à ARX | |
| de | Enzephalopathie, epileptische, ARX-assoziierte | |
| es | Encefalopatía epiléptica ligada a ARX | |
| it | Encefalopatia epilettica correlata ad ARX | |
| nl | ARX-gerelateerde epileptische encefalopathie | |
| pt | Encefalopatia epilética ARX-relacionada | |
| pl | Encefalopatia padaczkowa związana z ARX | |
| cs | ARX-vázaná epileptická encefalopatie | |
| uk | Епілептична енцефалопатія, повязана з ARX | |
| zh | ARX基因相关的癫痫性脑病 | |
| tr | ARX -ilişkili epileptik ensefalopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15921 | E | validated | |
| UMLS | C5680600 | E | validated |
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 (1):
- ORPHA:166472Monogenic disease with epilepsy
rare genetic diseases; rare neurological diseases
Children (5):
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/182079
- This record as JSON: /data/d/182079.json