Acute myeloid leukemia, t(16;21)(p11;q22)

Definition

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.)

Also known as AML, t(16;21)(p11;q22), AML, t(16;21)(p11.2;q22.2) — per MONDO