ORPHA:166463
Epilepsy syndrome
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Epilepsy syndrome | |
| fr | Syndrome épileptique | |
| de | Epileptische Syndrome | |
| es | Síndrome epiléptico | |
| it | Sindrome epilettica | |
| nl | Epileptisch syndroom | |
| pt | Síndrome epiléptico | |
| pl | Zespół padaczkowy | |
| cs | Epileptické syndromy | |
| uk | Синдром епілепсії | |
| zh | 癫痫综合征 | |
| tr | Epilepsi sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015650 | E | validated | |
| MONDO | 15650 | E | validated | |
| MeSH | D000073376 | E | validated | |
| UMLS | C4505072 | 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 (2):
- ORPHA:101998Rare epilepsy
rare neurological diseases - ORPHA:183512Rare genetic epilepsy
rare genetic diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:98260OBSOLETE: Adolescent-onset epilepsy syndrome referred to · inactive
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/166463
- This record as JSON: /data/d/166463.json