{"orpha":371433,"name":"Genetic periodic paralysis","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-371433/","orphanet_url":"https://www.orpha.net/en/disease/detail/371433","names":{"fr":{"name":"Paralysie périodique génétique"},"de":{"name":"Periodische Paralyse, genetisch bedingte"},"es":{"name":"Parálisis periódica genética"},"it":{"name":"Paralisi periodica genetica"},"nl":{"name":"Genetische periodieke paralyse","synonyms":["Genetische periodieke verlamming"]},"pt":{"name":"Paralisia periódica genética"},"pl":{"name":"Paraliż okresowy uwarunkowany genetycznie"},"cs":{"name":"Geneticky podmíněné periodické paralýzy"},"uk":{"name":"Генетично обумовлений періодичний параліч"},"zh":{"name":"遗传性周期性麻痹"},"tr":{"name":"Genetik periyodik paraliz"}},"xrefs":[{"source":"ICD-11","code":"8C74.1","qualifier":"NTBT","icd_relation":"specific","validated":true},{"source":"MONDO","code":"995","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681151","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":206634,"name":"Genetic skeletal muscle disease","classifications":[156]}],"children":[{"orpha":37553,"name":"Andersen-Tawil syndrome","type":"Disease"},{"orpha":682,"name":"Hyperkalemic periodic paralysis","type":"Disease"},{"orpha":681,"name":"Hypokalemic periodic paralysis","type":"Disease"},{"orpha":397750,"name":"Periodic paralysis with later-onset distal motor neuropathy","type":"Disease"},{"orpha":397755,"name":"Periodic paralysis with transient compartment-like syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}