{"orpha":77241,"name":"OBSOLETE: Lymphedema praecox","type":"Malformation syndrome","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 Meige disease","url":"https://raremap.alftech.space/d/ORPHA-77241/","orphanet_url":"https://www.orpha.net/en/disease/detail/77241","names":{"fr":{"name":"OBSOLETE : Lymphoedème précoce"},"de":{"name":"OBSOLET: Lymphoedema praecox"},"es":{"name":"OBSOLETO: Linfedema praecox"},"it":{"name":"OBSOLETO: Linfedema precoce"},"nl":{"name":"OBSOLEET: Lymphoedema praecox"},"pt":{"name":"OBSOLETO: Linfedema precoce"},"pl":{"name":"NIEAKTUALNE: Obrzek limfatyczny wczesny"},"cs":{"name":"NEAKTUÁLNÍ: Předčasný lymfedém"},"uk":{"name":"ЗАСТАРІЛО: Рання лімфедема"},"zh":{"name":"弃用：早发型淋巴水肿"},"tr":{"name":"Eski adı: Lenfödem prekoks"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":90186,"name":"Meige disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}