AML with recurrent genetic abnormalities | |
 AML with t(8;21)(q22;q22.1);RUNX1-RUNX1T1 | |
 AML with inv. (16)(p13.1q22) or t(16;16)(p13.1;q22);CBFB-MYH11 | |
 APL with PML-RARA | |
 AML with t(9;11)(p21.3;q23.3);MLLT3-KMT2A | |
 AML with t(6;9)(p23;q34.1);DEK-NUP214 | |
 AML with inv. (3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM | |
 AML (megakaryoblastic) with t(1;22)(p13.3;q13.3);RBM15-MKL1 | |
 Provisional entity: AML with BCR-ABL1 | |
 AML with mutated NPM1 | |
 AML with biallelic mutations of CEBPA | |
 Provisional entity: AML with mutated RUNX1 | |
AML with myelodysplasia-related changes | |
Therapy-related myeloid neoplasms | |
AML, NOS | |
 AML with minimal differentiation | |
 AML without maturation | |
 AML with maturation | |
 Acute myelomonocytic leukemia | |
 Acute monoblastic/monocytic leukemia | |
 Pure erythroid leukemia | |
 Acute megakaryoblastic leukemia | |
 Acute basophilic leukemia | |
 Acute panmyelosis with myelofibrosis | |
Myeloid sarcoma | |
Myeloid proliferations related to Down syndrome | |
 Transient abnormal myelopoiesis (TAM) | |
 Myeloid leukemia associated with Down syndrome |