{"orpha":728882,"name":"Esophageal atresia type B","type":"Clinical subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-728882/","orphanet_url":"https://www.orpha.net/en/disease/detail/728882","names":{"fr":{"name":"Atrésie de l'oesophage type B"},"de":{"name":"Ösophagusatresie Typ B"},"es":{"name":"Atresia esofágica tipo B"},"it":{"name":"Atresia esofagea tipo B"},"nl":{"name":"Atresie van oesofagus type B","synonyms":["Atresie van slokdarm type B"]},"pt":{"name":"Esophageal atresia, type B"},"pl":{"name":"Esophageal atresia type B"},"cs":{"name":"Esophageal atresia type B"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":1199,"name":"Esophageal atresia","classifications":[147,156,182]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":[],"prevalence":[],"phenotypes":null}