{"orpha":98750,"name":"Autoimmune neurological channelopathy","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-98750/","orphanet_url":"https://www.orpha.net/en/disease/detail/98750","names":{"fr":{"name":"Canalopathie neurologique auto-immune"},"de":{"name":"Ionenkanalkrankheit, autoimmune neurologische"},"es":{"name":"Canalopatía neurológica autoinmune"},"it":{"name":"Canalopatia neurologica autoimmune"},"nl":{"name":"Auto-immune neurologische kanalopathie"},"pt":{"name":"Canalopatia neurológica autoimune"},"pl":{"name":"Autoimmunologiczna kanałopatia neurologiczna"},"cs":{"name":"Autoimunitní neurologické kanálopatie"},"uk":{"name":"Аутоімунна неврологічна каналопатія"},"zh":{"name":"自身免疫性神经离子通道病"},"tr":{"name":"Otoimmün nörolojik kanalopati"}},"xrefs":[{"source":"UMLS","code":"C5681703","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98751,"name":"OBSOLETE: Autoimmune neurological channelopathy due to a p/q-type voltage gated calcium channel defect","status":"inactive"},{"type":"Referred to","orpha":98752,"name":"OBSOLETE: Autoimmune neurological channelopathy due to a potassium channel defect","status":"inactive"},{"type":"Referred to","orpha":98753,"name":"OBSOLETE: Autoimmune neurological channelopathy due to an acetylcholine receptor subunits defect","status":"inactive"}],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":71864,"name":"Muscular channelopathy","classifications":[181]}],"children":[{"orpha":581271,"name":"Cramp-fasciculation syndrome","type":"Disease"},{"orpha":84142,"name":"Isaacs syndrome","type":"Disease"},{"orpha":43393,"name":"Lambert-Eaton myasthenic syndrome","type":"Disease"},{"orpha":83467,"name":"Morvan syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}