{"orpha":719939,"name":"Central conducting lymphatic anomaly","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":["CCLA"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-719939/","orphanet_url":"https://www.orpha.net/en/disease/detail/719939","names":{"fr":{"name":"Anomalie lymphatique à drainage central"},"de":{"name":"Zentrale Lymphabflussstörung durch lymphatische Malformation","synonyms":["CCLA"]},"es":{"name":"Anomalía linfática del conducto central","synonyms":["CCLA"]},"it":{"name":"Anomalia linfatica del condotto centrale","synonyms":["CCLA"]},"nl":{"name":"Central conducting lymphatic anomaly","synonyms":["CCLA","Anomalie van centrale verzamelende lymfevaten"]},"pt":{"name":"Central conducting lymphatic anomaly"},"pl":{"name":"Central conducting lymphatic anomaly","synonyms":["CCLA"]},"cs":{"name":"Central conducting lymphatic anomaly","synonyms":["CCLA"]}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98028,"name":"Rare circulatory system disease"},"parents":[{"orpha":719950,"name":"Complex lymphatic anomaly","classifications":[147,198]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Adolescent","Adult","Childhood","Infancy"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}