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

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

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Aliases

• AML, inv(16)(p13.1;q22)
• AML, inv(16)(p13.1;q22.1)
• AML, inv(16)(p13.1q22)
• AML, inv(16)(p13.1q22.1)
• AML, inv(16)(p13;q22)
• AML, inv(16)(p13q22)