{"orpha":519270,"name":"Rare disorder with entropion","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-519270/","orphanet_url":"https://www.orpha.net/en/disease/detail/519270","names":{"fr":{"name":"Maladie rare avec entropion"},"de":{"name":"Seltene Erkrankung mit Entropium"},"es":{"name":"Trastorno raro con entropión"},"it":{"name":"Malattia rara con entropion"},"nl":{"name":"Zeldzame aandoening met entropion"},"pt":{"name":"Doença rara com entropion"},"pl":{"name":"Choroba rzadka z wywinięciem do wewnątrz (entropion) powieki"},"cs":{"name":"Vzácná porucha s entropiem"},"uk":{"name":"Рідкісний розлад з ентропіоном"},"zh":{"name":"罕见的眼睑内翻障碍"},"tr":{"name":"Entropiyon ileseyreden nadir hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681385","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98568,"name":"OBSOLETE: Congenital entropion","status":"inactive"},{"type":"Referred to","orpha":98569,"name":"OBSOLETE: Secondary entropion","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":98567,"name":"Rare eyelid malposition disorder","classifications":[147,189]}],"children":[{"orpha":519386,"name":"Isolated congenital entropion","type":"Morphological anomaly"},{"orpha":99170,"name":"Tarsal kink syndrome","type":"Morphological anomaly"},{"orpha":910,"name":"Xeroderma pigmentosum","type":"Disease"},{"orpha":90342,"name":"Xeroderma pigmentosum variant","type":"Disease"},{"orpha":220295,"name":"Xeroderma pigmentosum-Cockayne syndrome complex","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}