{"orpha":98576,"name":"Syndromic outer canthal malposition","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Malposition of external canthus"],"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-98576/","orphanet_url":"https://www.orpha.net/en/disease/detail/98576","names":{"fr":{"name":"Malposition canthale externe syndromique","synonyms":["Malposition canthale externe"]},"de":{"name":"Lidwinkel, externe Fehlstellung des"},"es":{"name":"Malposición externa de los cantos"},"it":{"name":"Malposizione esterna degli angoli palpebrali"},"nl":{"name":"Malpositie van canthus externus","synonyms":["Malpositie van buitenste ooghoek"]},"pt":{"name":"Má posição do canto externo"},"pl":{"name":"Nieprawidłowa pozycja zewnętrznego kąta oka","synonyms":["Malposition of external canthus"]},"cs":{"name":"Malpozice vnějšího očního koutku","synonyms":["Malposition of external canthus"]},"uk":{"name":"Синдромальне зовнішнє неправильне розташування зубів","synonyms":["Неправильне розташування зовнішнього канта"]},"zh":{"name":"综合征型外眼睑错位","synonyms":["外眦错位"]},"tr":{"name":"Sendromik dış kantüs malpozisyonu","synonyms":["Eksternal kanthusun malpozisyonu"]}},"xrefs":[{"source":"UMLS","code":"C5680327","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98567,"name":"Rare eyelid malposition disorder","classifications":[147,189]},{"orpha":522528,"name":"Rare genetic eyelid malposition disorder","classifications":[156]}],"children":[{"orpha":870,"name":"Down syndrome","type":"Malformation syndrome"},{"orpha":245,"name":"Nager syndrome","type":"Malformation syndrome"},{"orpha":648,"name":"Noonan syndrome","type":"Malformation syndrome"},{"orpha":2701,"name":"Noonan syndrome-like disorder with loose anagen hair","type":"Malformation syndrome"},{"orpha":861,"name":"Treacher-Collins syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}