{"orpha":506219,"name":"Rare disorder potentially indicated for hematopoietic stem cell transplant","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-506219/","orphanet_url":"https://www.orpha.net/en/disease/detail/506219","names":{"fr":{"name":"Maladie rare possiblement indiquée pour la transplantation de cellules souches hématopoïétiques"},"de":{"name":"Seltene Erkrankung zur potentiellen hämatopoetischen Stammzell-Transplantation indiziert"},"es":{"name":"Trastorno raro potencialmente indicado para trasplante de células madre hematopoyéticas"},"it":{"name":"Malattia rara con indicazione al trapianto di cellule staminali ematopoietiche"},"nl":{"name":"Zeldzame aandoening mogelijk geïndiceerd voor hematopoëtische stamceltransplantatie"},"pt":{"name":"Doença rara com potencial indicação para transplante de células tronco hematopoiéticas"},"pl":{"name":"Choroba rzadka będąca potencjalnym wskazaniem do przeszczepu hematopoetycznych komórek macierzystych"},"cs":{"name":"Vzácná porucha indikovaná k transplantaci hematopoetických kmenových buněk"},"uk":{"name":"Рідкісне захворювання, що є потенційним показанням для трансплантації гемопоетичних стовбурових клітин"},"zh":{"name":"可能适用于造血干细胞移植的罕见疾病"},"tr":{"name":"Hematopoietik kök hücre nakli için potansiyel olarak endike olan nadir bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681214","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":506207,"name":"Rare disorder potentially indicated for transplant","classifications":[233]}],"children":[{"orpha":437552,"name":"Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity","type":"Disease"},{"orpha":169090,"name":"Combined immunodeficiency due to CRAC channel dysfunction","type":"Disease"},{"orpha":221139,"name":"Combined immunodeficiency with facio-oculo-skeletal anomalies","type":"Disease"},{"orpha":436252,"name":"Combined immunodeficiency-multiple intestinal atresia","type":"Disease"},{"orpha":101987,"name":"Congenital neutropenia","type":"Category"},{"orpha":714493,"name":"Congenital thrombocytopenia-recurrent infections syndrome due to WIP deficiency","type":"Disease"},{"orpha":169346,"name":"DNA repair defect other than combined T-cell and B-cell immunodeficiencies","type":"Category"},{"orpha":309810,"name":"Disorder of peroxisomal alpha-, beta- and omega-oxidation","type":"Category"},{"orpha":658951,"name":"Early-onset immune dysregulation due to DOCK11 complete deficiency","type":"Disease"},{"orpha":370334,"name":"Extraskeletal Ewing sarcoma","type":"Disease"},{"orpha":3399,"name":"Germ cell tumor","type":"Category"},{"orpha":68364,"name":"Hemoglobinopathy","type":"Category"},{"orpha":98813,"name":"Hypohidrotic ectodermal dysplasia with immunodeficiency","type":"Disease"},{"orpha":169355,"name":"Immunodeficiency syndrome with autoimmunity","type":"Category"},{"orpha":331240,"name":"Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells","type":"Category"},{"orpha":171898,"name":"Lymphoid hemopathy","type":"Category"},{"orpha":79213,"name":"Mucopolysaccharidosis","type":"Category"},{"orpha":171895,"name":"Myeloid hemopathy","type":"Category"},{"orpha":480549,"name":"Non-severe combined immunodeficiency","type":"Clinical group"},{"orpha":2781,"name":"Osteopetrosis and related disorders","type":"Clinical group"},{"orpha":668,"name":"Osteosarcoma","type":"Disease"},{"orpha":158038,"name":"Primary hemophagocytic lymphohistiocytosis","type":"Clinical group"},{"orpha":182040,"name":"Rare aplastic anemia","type":"Category"},{"orpha":183660,"name":"Severe combined immunodeficiency","type":"Clinical group"},{"orpha":79225,"name":"Sphingolipidosis","type":"Category"},{"orpha":906,"name":"Wiskott-Aldrich syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}