{"orpha":522530,"name":"Rare genetic 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-522530/","orphanet_url":"https://www.orpha.net/en/disease/detail/522530","names":{"fr":{"name":"Maladie génétique rare avec entropion"},"de":{"name":"Seltene genetische Krankheit mit Entropion"},"es":{"name":"Trastorno genético raro con entropión"},"it":{"name":"Malattia genetica rara con entropion"},"nl":{"name":"Zeldzame genetische aandoening met entropion"},"pt":{"name":"Doença genética rara com entropion"},"pl":{"name":"Rzadka choroba z wywinięciem do wewnątrz (entropion) powiek uwarunkowana genetycznie"},"cs":{"name":"Vzácná genetická porucha s entropiem"},"uk":{"name":"Рідкісне генетично обумовлене захворювання з ентропією"},"zh":{"name":"罕见遗传性疾病伴眼睑内翻"},"tr":{"name":"Entropiyon ile seyreden nadir genetik bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681424","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":522528,"name":"Rare genetic eyelid malposition disorder","classifications":[156]}],"children":[{"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}