Any acute myeloid leukemia that has the chromosomal anomaly t(10;11)(p11.2;q23). (A cytogenetic abnormality that refers to the translocation of the short arm (p11.2) of chromosome 10 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/ABI1 fusions and acute myeloid leukemia.)
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childhood acute myeloid leukemia
MONDO:0004996
acute monocytic leukemia
MONDO:0007896
acute promyelocytic leukemia
MONDO:0012883
acute myeloid leukemia with t(8;21)(q22;q22) translocation
MONDO:0015166
acute myeloid leukemia by FAB classification
MONDO:0015667
inherited acute myeloid leukemia
MONDO:0017893