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Up to: Acute myeloid leukemia
Acute myeloid leukemia, t(10;11)(p12;q23)
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.)
This condition has no sub-types.