{"orpha":98687,"name":"Supranuclear eye movement disorder","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-98687/","orphanet_url":"https://www.orpha.net/en/disease/detail/98687","names":{"fr":{"name":"Maladie oculomotrice supranucléaire"},"de":{"name":"Paralyse, okulomotorische supranukleäre"},"es":{"name":"Parálisis supranuclear oculomotora"},"it":{"name":"Paralisi oculomotoria sopranucleare"},"nl":{"name":"Supranucleaire oculomotorische paralyse","synonyms":["Supranucleaire oculomotorische verlamming"]},"pt":{"name":"Paralisia oculomotora supranuclear"},"pl":{"name":"Nadjądrowe porażenie okoruchowe"},"cs":{"name":"Supranukleární obrny okohybných svalů"},"uk":{"name":"Супрануклеарний розлад руху очей"},"zh":{"name":"核上性眼球运动障碍"},"tr":{"name":"Supranükleer göz hareketi bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681698","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519341,"name":"Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature","classifications":[189]},{"orpha":522506,"name":"Rare genetic brainstem or cerebellar disorder with ophthalmic involvement as a major feature","classifications":[156]}],"children":[{"orpha":70472,"name":"Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type","type":"Disease"},{"orpha":306674,"name":"Kufor-Rakeb syndrome","type":"Disease"},{"orpha":506,"name":"Leigh syndrome","type":"Disease"},{"orpha":646,"name":"Niemann-Pick disease type C","type":"Disease"},{"orpha":683,"name":"Progressive supranuclear palsy","type":"Disease"},{"orpha":94147,"name":"Spinocerebellar ataxia type 7","type":"Disease"},{"orpha":905,"name":"Wilson disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}