{"orpha":98741,"name":"Neurological muscular channelopathy due to a genetic potassium channel defect","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-98741/","orphanet_url":"https://www.orpha.net/en/disease/detail/98741","names":{"fr":{"name":"Canalopathie neurologique génétique associée au canal potassique musculaire"},"de":{"name":"Ionenkanalkrankheit, neuromuskuläre, bei genetisch bedingtem Kaliumkanaldefekt"},"es":{"name":"Canalopatía neurológica muscular por un defecto genético de los canales de potasio"},"it":{"name":"Canalopatia neurologica genetica da difetto genetico del canale del potassio"},"nl":{"name":"Neurologische musculaire kanalopathie door een genetisch kaliumkanaaldefect"},"pt":{"name":"Canalopatia neurológica muscular por anomalia do canal de potássio"},"pl":{"name":"Neurologiczna kanałopatia mięśniowa z powodu genetycznego defektu kanału potasowego"},"cs":{"name":"Neurologická svalová kanálopatie způsobená genetickou poruchou draselného kanálu"},"uk":{"name":"Неврологічна мязова каналопатія внаслідок генетичного дефекту калієвих каналів"},"zh":{"name":"遗传性钾通道缺陷所致神经肌肉离子通道病"},"tr":{"name":"Genetik potasyum kanalı defektine bağlı nörolojik kas kanalopati"}},"xrefs":[{"source":"MONDO","code":"0957114","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681685","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":98737,"name":"Genetic neurological muscular channelopathy","classifications":[156,181]}],"children":[{"orpha":37553,"name":"Andersen-Tawil syndrome","type":"Disease"},{"orpha":972,"name":"Hereditary continuous muscle fiber activity","type":"Disease"},{"orpha":681,"name":"Hypokalemic periodic paralysis","type":"Disease"},{"orpha":36899,"name":"Myoclonus-dystonia syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}