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

MONDO:0100374

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.)

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)

2860 clinical trials for this condition and its sub-types.

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