Any acute myeloid leukemia that has the chromosomal anomaly t(16;21)(p11;q22). (A chromosomal translocation involving the FUS gene on chromosome 16p11 and the ERG gene on chromosome 21q22.)
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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