{"orpha":93942,"name":"OBSOLETE: Superior celosomia","type":"Morphological anomaly","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Syndromic diaphragmatic or abdominal wall malformation","url":"https://raremap.alftech.space/d/ORPHA-93942/","orphanet_url":"https://www.orpha.net/en/disease/detail/93942","names":{"fr":{"name":"OBSOLETE : Célosomie supérieure"},"de":{"name":"OBSOLET: Zölosomie, obere"},"es":{"name":"OBSOLETO: Celosomía superior"},"it":{"name":"OBSOLETO: Celosomia"},"nl":{"name":"OBSOLEET: Superieure celosomie"},"pt":{"name":"OBSOLETO: Celossomia"},"pl":{"name":"NIEAKTUALNE: Przepuklina pepkowa"},"cs":{"name":"NEAKTUÁLNÍ: Celosomie"},"uk":{"name":"ЗАСТАРІЛО: Вища целозомія"},"zh":{"name":"弃用：上部露脏畸形"},"tr":{"name":"Eski adı: Süperior selosomi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":108979,"name":"Syndromic diaphragmatic or abdominal wall malformation"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}