{"orpha":165805,"name":"Familial mesial temporal lobe epilepsy with febrile seizures","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Genetic epilepsy with febrile seizure plus","url":"https://raremap.alftech.space/d/ORPHA-165805/","orphanet_url":"https://www.orpha.net/en/disease/detail/165805","names":{"fr":{"name":"Epilepsie temporale mésiale familiale avec convulsions fébriles"},"de":{"name":"Temporallappenepilepsie, mesiale, mit Fieberkrämpfen, familiäre Form"},"es":{"name":"Epilepsia familiar mesial temporal con crisis febriles"},"it":{"name":"Epilessia mesiale temporale familiare con convulsioni febbrili"},"nl":{"name":"Familiale mesiale temporaalkwabepilepsie met febriele epileptische aanvallen"},"pt":{"name":"Epilepsia temporal mesial familiar com convulsões febris"},"pl":{"name":"Rodzinna padaczka przyśrodkowego płata skroniowego z drgawkami gorączkowymi"},"cs":{"name":"Familiární meziální epilepsie spánkového laloku s febrilními záchvaty","synonyms":["Familiární epileptický syndrom","Generalizovaná epilepsie s febrilními záchvaty"]},"uk":{"name":"Сімейна мезіальна скронева епілепсія з фебрильними нападами","definition":"A rare, genetic, familial partial epilepsy disease characterized by simple partial seizures, complex partial seizures and/or secondarily generalized seizures, originating from the inner aspect of the temporal lobe, associated with an antecedant history of febrile seizures, ocurring in various members of a family. Hippocampal abnormalities (e.g. hippocampal sclerosis) may also be associated."},"zh":{"name":"家族性近中颞叶癫痫伴发热性惊厥发作","definition":"一种罕见的遗传性家族性局限性癫痫疾病，其特征是单纯部分性癫痫发作、复杂部分性癫痫发作和/或继发性全身性癫痫发作，起源于颞叶内侧，与热性惊厥史有关，发生于一个家庭的不同成员中。该病也可能伴海马异常(如海马硬化)。"},"tr":{"name":"Ateşli nöbetler ile seyreden ailesel mezyal temporal lob epilepsisi"}},"xrefs":[{"source":"MONDO","code":"0013742","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5191318","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":36387,"name":"Genetic epilepsy with febrile seizure plus"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}