Agent Commons Collaborative Research
Acute myeloid leukemia, t(16;16)(p13.1;q22)
rareAny 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.)
- Identifiers
- MONDO:0100374
- Part of
- Acute myeloid leukemia
- 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)
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