{"orpha":2416,"name":"Congenital primary lymphedema without systemic or visceral involvement","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-2416/","orphanet_url":"https://www.orpha.net/en/disease/detail/2416","names":{"fr":{"name":"Lymphoedème primaire congénital sans atteinte systémique ou viscérale"},"de":{"name":"Kongenitales primäres Lymphödem ohne systemische oder viszerale Beteiligung"},"es":{"name":"Linfedema congénito primario con afectación sistémica o visceral"},"it":{"name":"Linfedema primitivo congenito"},"nl":{"name":"Congenitaal primair lymfoedeem zonder systemische of viscerale betrokkenheid"},"pt":{"name":"Linfedema primário congénito sem envolvimento sistémico ou visceral"},"pl":{"name":"Wrodzony pierwotny obrzęk limfatyczny"},"cs":{"name":"Vrozený primární lymfedém bez systémového či orgánového postižení"},"uk":{"name":"Вроджена первинна лімфедема без системного або вісцерального ураження"},"zh":{"name":"先天性原发性淋巴水肿不伴系统性或内脏受累"},"tr":{"name":"Sistemik veya viseral tutulum olmayan doğumsal primer lenfödem"}},"xrefs":[{"source":"UMLS","code":"C5680523","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":568041,"name":"Primary lymphedema without systemic or visceral involvement","classifications":[147,156,187,198]}],"children":[{"orpha":295000,"name":"Amniotic band syndrome","type":"Malformation syndrome"},{"orpha":569821,"name":"Congenital primary lymphedema of Gordon","type":"Disease"},{"orpha":2077,"name":"German syndrome","type":"Malformation syndrome"},{"orpha":2526,"name":"Microcephaly-chorioretinopathy-lymphedema syndrome","type":"Malformation syndrome"},{"orpha":79452,"name":"Milroy disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}