Any acute myeloid leukemia that has the chromosomal anomaly t(9;11)(p21.3;q23.3). (A cytogenetic abnormality that refers to the translocation of the short arm (p21.3) of chromosome 9 and the long arm (q23.3) of chromosome 11. It is associated with the development of acute myeloid leukemia with the MLLT3-MLL fusion gene transcript.)
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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