{"orpha":182083,"name":"Channelopathy with epilepsy","type":"Category","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-182083/","orphanet_url":"https://www.orpha.net/en/disease/detail/182083","names":{"fr":{"name":"Canalopathie avec épilepsie"},"de":{"name":"Ionenkanalkrankheit mit Epilepsie"},"es":{"name":"Canalopatía con epilepsia"},"it":{"name":"Canalopatia associata a epilessia"},"nl":{"name":"Kanalopathie met epilepsie"},"pt":{"name":"Canalopatia com epilepsia"},"pl":{"name":"Kanałopatia z padaczką"},"cs":{"name":"Kanálopatie s epilepsií"},"uk":{"name":"Каналопатія з епілепсією"},"zh":{"name":"离子通道病伴癫痫"},"tr":{"name":"Epilepsi ile seyreden kanalopati"}},"xrefs":[{"source":"MONDO","code":"15922","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680595","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":166472,"name":"Monogenic disease with epilepsy","classifications":[156,181]}],"children":[{"orpha":33069,"name":"Dravet syndrome","type":"Disease"},{"orpha":199343,"name":"EAST syndrome","type":"Disease"},{"orpha":1934,"name":"Early infantile developmental and epileptic encephalopathy","type":"Clinical syndrome"},{"orpha":293181,"name":"Epilepsy of infancy with migrating focal seizures","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}