Any acute myeloid leukemia that has the chromosomal anomaly t(16;16)(p13.1;q22). (A chromosomal translocation that involves chromosome 16. It is often associated with the development of acute myeloid leukemia CBFB-MYH11, acute myelomonocytic leukemia with abnormal eosinophils, and granulocytic sarcoma.). The disease is acute myeloid leukemia, t(16;16)(p13.1;q22) (MONDO_0100374, a Monarch Disease Ontology term). Also known as: AML, t(16;16)(p13.1;q22), AML, t(16;16)(p13.1;q22.1), AML, t(16;16)(p13.1q22), AML, t(16;16)(p13.1q22.1), AML, t(16;16)(p13;q22), AML, t(16;16)(p13q22).