Any acute myeloid leukemia that has the chromosomal anomaly t(10;11)(p12;q23). (A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood.). The disease is MONDO_0100377 (acute myeloid leukemia, t(10;11)(p12;q23)). Also known as: AML, t(10;11)(p12;q23).