ORPHA:699645
Variable age-onset epilepsy syndrome
- 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.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Variable age-onset epilepsy syndrome | |
| fr | Syndrome épileptique avec âge de début variable | |
| de | Epilepsiesyndrom mit variablem Erkrankungsalter | |
| es | Síndrome epiléptico con edad de inicio variable | |
| it | Sindrome epilettica con età d'esordio variabile | |
| nl | Epilepsiesyndroom met variabele aanvangsleeftijd | |
| pt | Variable age-onset epilepsy syndrome | |
| pl | Variable age-onset epilepsy syndrome | |
| cs | Variable age-onset epilepsy syndrome |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:166463Epilepsy syndrome
rare genetic diseases; rare neurological diseases
Children (10):
- ORPHA:101046Epilepsy with auditory features
- ORPHA:698005Epilepsy with generalized tonic-clonic seizures alone
- ORPHA:86814Familial adult myoclonic epilepsy
- ORPHA:98820Familial focal epilepsy with variable foci
- ORPHA:1941Juvenile absence epilepsy
- ORPHA:307Juvenile myoclonic epilepsy
- ORPHA:98261Progressive myoclonic epilepsy
- ORPHA:1929Rasmussen syndrome
- ORPHA:310Reflex epilepsy
- ORPHA:98784Sleep-related hypermotor epilepsy
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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/699645
- This record as JSON: /data/d/699645.json