{"orpha":98737,"name":"Genetic neurological 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-98737/","orphanet_url":"https://www.orpha.net/en/disease/detail/98737","names":{"fr":{"name":"Canalopathie neurologique musculaire génétique"},"de":{"name":"Ionenkanalkrankheit, neuromuskuläre, genetisch bedingte"},"es":{"name":"Canalopatía neurológica muscular genética"},"it":{"name":"Canalopatia muscolare genetica"},"nl":{"name":"Genetische neurologische musculaire kanalopathie"},"pt":{"name":"Canalopatia neurológica muscular genética"},"pl":{"name":"Genetyczna neurologiczna kanałopatia mięśniowa"},"cs":{"name":"Genetické neurologické svalové kanálopatie"},"uk":{"name":"Генетично обумовлена неврологічна мязова каналопатія"},"zh":{"name":"遗传性神经肌肉通道病"},"tr":{"name":"Genetik nörolojik kas kanalpati"}},"xrefs":[{"source":"UMLS","code":"C5681683","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":352298,"name":"OBSOLETE: Genetic muscular channelopathy","status":"inactive"}],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":183497,"name":"Genetic neuromuscular disease","classifications":[156]},{"orpha":71864,"name":"Muscular channelopathy","classifications":[181]}],"children":[{"orpha":98740,"name":"Neurological muscular channelopathy due to a genetic calcium channel defect","type":"Category"},{"orpha":98739,"name":"Neurological muscular channelopathy due to a genetic chloride channel defect","type":"Category"},{"orpha":98741,"name":"Neurological muscular channelopathy due to a genetic potassium channel defect","type":"Category"},{"orpha":98742,"name":"Neurological muscular channelopathy due to a genetic ryanodine receptor defect","type":"Category"},{"orpha":98738,"name":"Neurological muscular channelopathy due to a genetic sodium channel defect","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}