Any acute myeloid leukemia that has the chromosomal anomaly t(6;9)(p23;q34.1). (A cytogenetic abnormality that refers to the translocation of the short arm (p23) of chromosome 6 and the long arm (q34.1) of chromosome 9. It is associated with DEK/NUP214 fusions, acute myeloid leukemia and myelodysplastic syndromes.). The disease is MONDO_0100382 (acute myeloid leukemia, t(6;9)(p23;q34.1)). Also known as: AML, t(6;9)(p22.3;q34.1), AML, t(6;9)(p22;q34), AML, t(6;9)(p23;q34), AML, t(6;9)(p23;q34.1).