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

Definition

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;q22), AML, t(16;16)(p13.1;q22.1), AML, t(16;16)(p13.1;q22), AML, t(16;16)(p13.1q22.1), AML, t(16;16)(p13.1q22), AML, t(16;16)(p13q22) — per MONDO

Also identified as

• NCIT C9019 per MONDO

Affected Organs