{"orpha":98571,"name":"Secondary 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-98571/","orphanet_url":"https://www.orpha.net/en/disease/detail/98571","names":{"fr":{"name":"Ectropion secondaire"},"de":{"name":"Ektropium, sekundäres"},"es":{"name":"Ectropión secundario"},"it":{"name":"Ectropion secondario"},"nl":{"name":"Secundair ectropion"},"pt":{"name":"Ectropion secundário"},"pl":{"name":"Wtórne wywinięcie powiek - ektropion"},"cs":{"name":"Sekundární ektropia"},"uk":{"name":"Вторинний ектропіон"},"zh":{"name":"继发性眼睑外翻"},"tr":{"name":"Sekonder ektropiyon"}},"xrefs":[{"source":"ICD-10","code":"H02.1","qualifier":"E","icd_relation":"specific","validated":true},{"source":"UMLS","code":"C5681652","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519268,"name":"Rare disorder with ectropion","classifications":[147,156,189]}],"children":[{"orpha":281097,"name":"Autosomal recessive congenital ichthyosis","type":"Clinical group"},{"orpha":1231,"name":"Barber-Say syndrome","type":"Malformation syndrome"},{"orpha":870,"name":"Down syndrome","type":"Malformation syndrome"},{"orpha":2269,"name":"Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome","type":"Disease"},{"orpha":246,"name":"Postaxial acrofacial dysostosis","type":"Malformation syndrome"},{"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}