{"orpha":2415,"name":"Rare lymphatic malformation","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["LM","Lymphangioma"],"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-2415/","orphanet_url":"https://www.orpha.net/en/disease/detail/2415","names":{"fr":{"name":"Malformation lymphatique rare","synonyms":["Lymphangiome","ML"]},"de":{"name":"Seltene lymphatische Fehlbildung","synonyms":["LM","Lymphangiom","Lymphatische Malformation"]},"es":{"name":"Malformación linfática rara","synonyms":["Linfangioma"]},"it":{"name":"Malformazione linfatica rara","synonyms":["Linfangioma","ML"]},"nl":{"name":"Zeldzame lymfatische malformatie","synonyms":["Zeldzame malformatie van lymfestelsel","LM","Lymfangioom"]},"pt":{"name":"Malformação linfática rara isolada","synonyms":["LM","Linfangioma"]},"pl":{"name":"Izolowana rzadka malformacja limfatyczna","synonyms":["Limfangioma","LM"]},"cs":{"name":"Vzácná lymfatická malformace","synonyms":["LM","Lymfangiom"]},"uk":{"name":"Рідкісна лімфатична мальформація","synonyms":["LM","Лімфангіома"]},"zh":{"name":"罕见淋巴管畸形","synonyms":["淋巴管瘤"]},"tr":{"name":"Nadir lenfatik malformasyon","synonyms":["LM","Lenfanjiyom"]}},"xrefs":[{"source":"ICD-10","code":"D18.1","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"LA90.1","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1456264474"},{"source":"MONDO","code":"2013","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5575909","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"9789","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":137923,"name":"OBSOLETE: Cervicofacial lymphatic malformation","status":"inactive"}],"preferential_parent":{"orpha":98028,"name":"Rare circulatory system disease"},"parents":[{"orpha":211255,"name":"Slow-flow malformation, lymphatic type","classifications":[147,198]}],"children":[{"orpha":719931,"name":"Angiokeratoma circumscriptum","type":"Morphological anomaly"},{"orpha":719950,"name":"Complex lymphatic anomaly","type":"Clinical group"},{"orpha":458833,"name":"Isolated lymphatic malformation","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Infancy","Neonatal"],"prevalence":[{"type":"Point prevalence","qualification":"Value and class","class":"1-5 / 10 000","value":12.5,"area":"Europe","status":"Validated","source":"ORPHANET"}],"phenotypes":null}