{"orpha":568044,"name":"Primary lymphedema with systemic or visceral involvement","type":"Category","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-568044/","orphanet_url":"https://www.orpha.net/en/disease/detail/568044","names":{"fr":{"name":"Lymphoedème primaire avec atteinte systémique ou viscérale"},"de":{"name":"Primäres Lymphödem mit systemischer und viszeraler Beteiligung"},"es":{"name":"Linfedema primario con afectación sistémica o visceral"},"it":{"name":"Linfedema primitivo sistemico o viscerale"},"nl":{"name":"Primair lymfoedeem met systemische of viscerale betrokkenheid"},"pt":{"name":"Linfedema primário com envolvimento sistémico ou visceral"},"pl":{"name":"Pierwotny obrzęk limfatyczny ze zmianami układowymi lub trzewnymi"},"cs":{"name":"Primární lymfedém se systémovým nebo viscerálním postižením"},"uk":{"name":"Первинна лімфедема із системним або вісцеральним ураженням"},"zh":{"name":"全身或内脏受累型原发性淋巴水肿"},"tr":{"name":"Sistemik veya viseral tutulum ile seyreden primer lenfödem"}},"xrefs":[{"source":"UMLS","code":"C5681304","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":77240,"name":"Primary lymphedema","classifications":[147,156,187,198]}],"children":[{"orpha":1116,"name":"Aplasia cutis congenita-intestinal lymphangiectasia syndrome","type":"Disease"},{"orpha":1563,"name":"Dahlberg-Borer-Newcomer syndrome","type":"Malformation syndrome"},{"orpha":568065,"name":"EPHB4-related lymphatic-related hydrops fetalis","type":"Disease"},{"orpha":2136,"name":"Hennekam syndrome","type":"Malformation syndrome"},{"orpha":69735,"name":"Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome","type":"Disease"},{"orpha":662,"name":"Lymphedema with yellow nails","type":"Disease"},{"orpha":86915,"name":"Lymphedema-atrial septal defects-facial changes syndrome","type":"Malformation syndrome"},{"orpha":568062,"name":"PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis","type":"Disease"},{"orpha":568056,"name":"Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}