{"orpha":88993,"name":"Esophageal malformation","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Malformation of the esophagus"],"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-88993/","orphanet_url":"https://www.orpha.net/en/disease/detail/88993","names":{"fr":{"name":"Malformation de l'oesophage","synonyms":["Malformation oesophagienne"]},"de":{"name":"Ösophagusfehlbildung","synonyms":["Fehlbildung der Speiseröhre"]},"es":{"name":"Malformación esofágica","synonyms":["Malformación del esófago"]},"it":{"name":"Malformazione esofagea congenita"},"nl":{"name":"Oesofageale malformatie","synonyms":["Malformatie van oesofagus","Malformatie van slokdarm"]},"pt":{"name":"Malformação esofágica","synonyms":["Malformação do esófago"]},"pl":{"name":"Malformacja przełyku","synonyms":["Malformation of the esophagus"]},"cs":{"name":"Malformace jícnu","synonyms":["Malformation of the esophagus"]},"uk":{"name":"Вади розвитку стравоходу"},"zh":{"name":"食管畸形"},"tr":{"name":"Özofagus malformasyonu"}},"xrefs":[{"source":"ICD-11","code":"LB12","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1999264345"},{"source":"UMLS","code":"C5681451","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98039,"name":"Digestive tract malformation","classifications":[147,182]},{"orpha":183545,"name":"Genetic digestive tract malformation","classifications":[156]}],"children":[{"orpha":371445,"name":"Genetic syndromic esophageal malformation","type":"Category"},{"orpha":108959,"name":"Non-syndromic esophageal malformation","type":"Category"},{"orpha":108961,"name":"Syndromic esophageal malformation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}