Catalog
Acute myeloid leukaemia with recurrent genetic abnormalities
Link to WHO Definition
Acute myeloid leukaemia with recurrent genetic abnormalities – http://id.who.int/icd/entity/1430965006
Parents
Children
- Acute myeloid leukemia with t(8;21)(q22;q22) translocation
- Acute promyelocytic leukaemia with t(15;17)(q24.1;q21.1), PML-RARA
- Acute myeloid leukaemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1
- Acute myeloid leukaemia with t(6;9)(p23;q34); DEK- NUP214
- Acute myeloid leukaemia with mutated NPM1
- Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22), CBFB-MYH11
- Acute myeloid leukaemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1
- Acute myeloid leukaemia with t(8;21)(q22;q22), RUNX1-RUNX1T1
- Acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL
- Acute myeloid leukaemia with mutated CEBPA
- Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)