{"orpha":309,"name":"OBSOLETE: Familial partial epilepsy","type":"Clinical group","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Childhood-onset epilepsy syndrome","url":"https://raremap.alftech.space/d/ORPHA-309/","orphanet_url":"https://www.orpha.net/en/disease/detail/309","names":{"fr":{"name":"OBSOLETE : Epilepsie partielle familiale"},"de":{"name":"OBSOLET: Familiäre partielle Epilepsie"},"es":{"name":"OBSOLETO: Epilepsia parcial familiar"},"it":{"name":"OBSOLETO: Epilessia parziale familiare"},"nl":{"name":"OBSOLEET: Familiale partiële epilepsie"},"pt":{"name":"OBSOLETO: Epilepsia parcial familiar"},"pl":{"name":"NIEAKTUALNE: Rodzinna padaczka częściowa"},"cs":{"name":"NEAKTUÁLNÍ: Familiární parciální epilepsie"},"uk":{"name":"Сімейна парціальна епілепсія"},"zh":{"name":"家族性部分性癫痫"},"tr":{"name":"ailesel kısmi epilepsi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98259,"name":"Childhood-onset epilepsy syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}