{"orpha":71864,"name":"Muscular 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-71864/","orphanet_url":"https://www.orpha.net/en/disease/detail/71864","names":{"fr":{"name":"Canalopathie musculaire"},"de":{"name":"Ionenkanalkrankheit, muskuläre"},"es":{"name":"Canalopatía muscular"},"it":{"name":"Canalopatia muscolare"},"nl":{"name":"Musculaire kanalopathie"},"pt":{"name":"Canalopatia muscular"},"pl":{"name":"Kanałopatia plamki"},"cs":{"name":"Svalové kanálopatie"},"uk":{"name":"Мязова каналопатія"},"zh":{"name":"肌肉离子通道病"},"tr":{"name":"Kas kanalopatisi"}},"xrefs":[{"source":"MONDO","code":"0019119","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19119","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681306","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":68381,"name":"Neuromuscular disease","classifications":[181]}],"children":[{"orpha":98750,"name":"Autoimmune neurological channelopathy","type":"Category"},{"orpha":98737,"name":"Genetic neurological muscular channelopathy","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}