{"orpha":699645,"name":"Variable age-onset epilepsy syndrome","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-699645/","orphanet_url":"https://www.orpha.net/en/disease/detail/699645","names":{"fr":{"name":"Syndrome épileptique avec âge de début variable"},"de":{"name":"Epilepsiesyndrom mit variablem Erkrankungsalter"},"es":{"name":"Síndrome epiléptico con edad de inicio variable"},"it":{"name":"Sindrome epilettica con età d'esordio variabile"},"nl":{"name":"Epilepsiesyndroom met variabele aanvangsleeftijd"},"pt":{"name":"Variable age-onset epilepsy syndrome"},"pl":{"name":"Variable age-onset epilepsy syndrome"},"cs":{"name":"Variable age-onset epilepsy syndrome"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":166463,"name":"Epilepsy syndrome","classifications":[156,181]}],"children":[{"orpha":101046,"name":"Epilepsy with auditory features","type":"Disease"},{"orpha":698005,"name":"Epilepsy with generalized tonic-clonic seizures alone","type":"Disease"},{"orpha":86814,"name":"Familial adult myoclonic epilepsy","type":"Disease"},{"orpha":98820,"name":"Familial focal epilepsy with variable foci","type":"Disease"},{"orpha":1941,"name":"Juvenile absence epilepsy","type":"Disease"},{"orpha":307,"name":"Juvenile myoclonic epilepsy","type":"Disease"},{"orpha":98261,"name":"Progressive myoclonic epilepsy","type":"Clinical group"},{"orpha":1929,"name":"Rasmussen syndrome","type":"Disease"},{"orpha":310,"name":"Reflex epilepsy","type":"Clinical group"},{"orpha":98784,"name":"Sleep-related hypermotor epilepsy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}