{"orpha":522526,"name":"Rare genetic palpebral 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-522526/","orphanet_url":"https://www.orpha.net/en/disease/detail/522526","names":{"fr":{"name":"Maladie génétique rare de la paupière"},"de":{"name":"Seltene genetische Krankheit des Augenlids"},"es":{"name":"Trastorno palpebral genético raro"},"it":{"name":"Malattia genetica rara della palpebra"},"nl":{"name":"Zeldzame genetische palpebrale aandoening","synonyms":["Zeldzame genetische aandoening van ooglid"]},"pt":{"name":"Doença palpebral genética rara"},"pl":{"name":"Rzadka choroba powiek uwarunkowana genetycznie"},"cs":{"name":"Vzácná genetická palpebrální porucha"},"uk":{"name":"Рідкісне генетично обумовлене пальпебральне захворювання"},"zh":{"name":"罕见遗传性眼睑疾病"},"tr":{"name":"Nadir genetik palpebral bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681426","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183557,"name":"Genetic developmental defect of the eye","classifications":[156]},{"orpha":522524,"name":"Rare genetic disorder of the ocular adnexa","classifications":[156]}],"children":[{"orpha":98561,"name":"Congenital malformation of the eyelid","type":"Category"},{"orpha":522528,"name":"Rare genetic eyelid malposition disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}