Acute myeloid leukemia, t(16;16)(p13.1;q22)

From BugSigDB

Any acute myeloid leukemia that has the chromosomal anomaly t(16;16)(p13.1;q22). (A chromosomal translocation that involves chromosome 16. It is often associated with the development of acute myeloid leukemia CBFB-MYH11, acute myelomonocytic leukemia with abnormal eosinophils, and granulocytic sarcoma.)
  • AML, t(16;16)(p13.1;q22)
  • AML, t(16;16)(p13.1;q22.1)
  • AML, t(16;16)(p13.1q22)
  • AML, t(16;16)(p13.1q22.1)
  • AML, t(16;16)(p13;q22)
  • AML, t(16;16)(p13q22)