{"orpha":98570,"name":"Congenital ectropion","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-98570/","orphanet_url":"https://www.orpha.net/en/disease/detail/98570","names":{"fr":{"name":"Ectropion congénital"},"de":{"name":"Ektropium, kongenitales"},"es":{"name":"Ectropión congénita"},"it":{"name":"Ectropion congenito"},"nl":{"name":"Congenitaal ectropion"},"pt":{"name":"Ectropion congénito"},"pl":{"name":"Wrodzone wywinięcie powiek - ektropion"},"cs":{"name":"Vrozená ektropia"},"uk":{"name":"Вроджений ектропіон"},"zh":{"name":"先天性眼睑外翻"},"tr":{"name":"Doğumsal ektropiyon"}},"xrefs":[{"source":"ICD-10","code":"Q10.1","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"LA14.03","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"945558601"},{"source":"MONDO","code":"0020161","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0266578","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":519268,"name":"Rare disorder with ectropion","classifications":[147,156,189]}],"children":[{"orpha":1997,"name":"Blepharo-cheilo-odontic syndrome","type":"Malformation syndrome"},{"orpha":99171,"name":"Isolated congenital ectropion","type":"Morphological anomaly"},{"orpha":2322,"name":"Kabuki syndrome","type":"Malformation syndrome"},{"orpha":357158,"name":"Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}