Conditions / Other

acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)

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An acute myeloid leukemia that is characterized by the presence of abnormal bone marrow eosinophils and the characteristic cytogenetic abnormality inv(16)(p13.1q22) or t(16;16)(p13.1;q22), which results in the expression of the fusion protein CBFB-MYH11.

Also known as: Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11; acute myeloid leukemia with abnormal marrow eosinophils