{"orpha":90053,"name":"Complications after hematopoietic stem cell transplantation","type":"Particular clinical situation in a disease or syndrome","group":"Disorder","status":"active","flags":[],"synonyms":["Complications after HSCT"],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-90053/","orphanet_url":"https://www.orpha.net/en/disease/detail/90053","names":{"fr":{"name":"Complications après transplantation de cellules souches hématopoïétiques"},"de":{"name":"Komplikationen nach hämatopoetischer Stammzell-Transplantation","synonyms":["Komplikationen nach HSCT"]},"es":{"name":"Complicaciones post-trasplante de células madre hematopoyéticas","synonyms":["Complicaciones post-TCMH"]},"it":{"name":"Trapianto di cellule staminali ematopoietiche"},"nl":{"name":"Complicaties na hematopoëtische stamceltransplantatie","synonyms":["Complicaties na HSCT"]},"pt":{"name":"Transplantação de células hematopoiéticas"},"pl":{"name":"Transplantacja komórek hematopoetycznych","synonyms":["Complications after HSCT"]},"cs":{"name":"Transplantace krvetvorných kmenových buněk","synonyms":["Complications after HSCT"]},"uk":{"name":"Ускладнення після трансплантації гемопоетичних стовбурових клітин","synonyms":["Ускладнення після ТГСК"]},"zh":{"name":"造血干细胞移植术后并发症","synonyms":["HSCT后并发症"]},"tr":{"name":"Hematopoetik kök hücre nakli sonrası komplikasyonlar","synonyms":["HSCT sonrası komplikasyonlar"]}},"xrefs":[{"source":"ICD-10","code":"Z94.8","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"NE8Y","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"UMLS","code":"C5680176","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":565779,"name":"Rare disorder potentially indicated for transplant or complication after transplantation"},"parents":[{"orpha":565779,"name":"Rare disorder potentially indicated for transplant or complication after transplantation","classifications":[233]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["All ages"],"prevalence":[{"type":"Point prevalence","qualification":"Value and class","class":"1-9 / 1 000 000","value":0.65,"area":"Europe","status":"Validated","source":"European Medicines Agency[OTHER]"}],"phenotypes":null}