Acute myeloid leukemia, t(16;16)(p13.1;q22)
MONDO:0100374Any 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.)
Also known as: 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)
3097 clinical trials for this condition and its sub-types, 10 tagged with Acute myeloid leukemia, t(16;16)(p13.1;q22) itself.
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