{"orpha":98277,"name":"Acute myeloid leukemia with recurrent genetic anomaly","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["AML with recurrent genetic anomaly"],"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-98277/","orphanet_url":"https://www.orpha.net/en/disease/detail/98277","names":{"fr":{"name":"Leucémie aiguë myéloïde avec anomalie génétique récurrente"},"de":{"name":"Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie","synonyms":["AML mit rekurrenter genetischer Anomalie"]},"es":{"name":"Leucemia mieloide aguda con anomalía genética recurrente","synonyms":["LMA con anomalías genéticas recurrentes"]},"it":{"name":"Leucemia mieloide acuta con anomalia genetica ricorrente","synonyms":["AML con anomalia genetica ricorrente"]},"nl":{"name":"Acute myeloïde leukemie met terugkerende genetische anomalie","synonyms":["AML met terugkerende genetische anomalie"]},"pt":{"name":"Leucemia mielóide aguda com anomalias genéticas recorrentes"},"pl":{"name":"Ostra białaczka szpikowa z powracającą wadą genetyczną","synonyms":["AML z powracającą wadą genetyczną"]},"cs":{"name":"Akutní myeloidní leukémie s rekurentními genetickými abnormalitami","synonyms":["AML s rekurentními genetickými abnormalitami"]},"uk":{"name":"Гостра мієлоїдна лейкемія з рецидивуючою генетичною аномалією","synonyms":["ГМЛ з рецидивуючою генетичною аномалією"]},"zh":{"name":"急性髓系白血病伴重现性遗传学异常","synonyms":["AML伴复发性遗传学异常"]},"tr":{"name":"Tekrarlayan genetik anomali ile seyreden akut miyeloid lösemi","synonyms":["Tekrarlayan genetik anomalili AML"]}},"xrefs":[{"source":"OMIM","code":"601626","qualifier":"NTBT","icd_relation":null,"validated":true},{"source":"ICD-11","code":"2A60.0","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1430965006"},{"source":"UMLS","code":"C4303425","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"12758","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":519,"name":"Acute myeloid leukemia","classifications":[194,202,233]}],"children":[{"orpha":98831,"name":"Acute myeloid leukemia with 11q23 abnormalities","type":"Disease"},{"orpha":319480,"name":"Acute myeloid leukemia with CEBPA somatic mutations","type":"Disease"},{"orpha":402026,"name":"Acute myeloid leukemia with NPM1 somatic mutations","type":"Disease"},{"orpha":98829,"name":"Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)","type":"Disease"},{"orpha":402020,"name":"Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)","type":"Disease"},{"orpha":402014,"name":"Acute myeloid leukemia with t(6;9)(p23;q34)","type":"Disease"},{"orpha":370026,"name":"Acute myeloid leukemia with t(8;16)(p11;p13) translocation","type":"Disease"},{"orpha":102724,"name":"Acute myeloid leukemia with t(8;21)(q22;q22) translocation","type":"Disease"},{"orpha":402017,"name":"Acute myeloid leukemia with t(9;11)(p22;q23)","type":"Disease"},{"orpha":585867,"name":"Acute myeloid leukemia with t(9;22)(q34.1;q11.2)","type":"Disease"},{"orpha":520,"name":"Acute promyelocytic leukemia","type":"Disease"},{"orpha":402023,"name":"Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[{"type":"Annual incidence","qualification":"Value and class","class":"1-9 / 1 000 000","value":0.11,"area":"Europe","status":"Validated","source":"RARECARE surveillance of rare cancers in Europe[OTHER]"}],"phenotypes":null}