{"orpha":209978,"name":"Alternating hemiplegia","type":"Clinical group","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-209978/","orphanet_url":"https://www.orpha.net/en/disease/detail/209978","names":{"fr":{"name":"Hémiplégie alternante"},"de":{"name":"Hemiplegie, alternierende"},"es":{"name":"Hemiplejia alternante"},"it":{"name":"Emiplegia alternante"},"nl":{"name":"Alternerende hemiplegie"},"pt":{"name":"Hemiplegia alternante"},"pl":{"name":"Naprzemienne porażenie połowicze"},"cs":{"name":"Alternující hemiplegie"},"uk":{"name":"Альтернуюча геміплегія"},"zh":{"name":"交叉性肢体瘫痪"},"tr":{"name":"Alternatif hemipleji"}},"xrefs":[{"source":"ICD-11","code":"MB53.0","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"774373615"},{"source":"MONDO","code":"0016210","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16210","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0278110","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":166472,"name":"Monogenic disease with epilepsy","classifications":[156,181]},{"orpha":71859,"name":"Rare genetic neurological disorder","classifications":[156]},{"orpha":98006,"name":"Rare neurologic disease","classifications":[181]}],"children":[{"orpha":2131,"name":"Alternating hemiplegia of childhood","type":"Disease"},{"orpha":209973,"name":"Benign nocturnal alternating hemiplegia of childhood","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}