t(16;16)(p13.1;q22)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** 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.

**Synonyms:** - t(16;16)(p13.1;q22.1) - t(16;16)(p13.1q22) - t(16;16)(p13.1q22.1) - t(16;16)(p13;q22) - t(16;16)(p13q22)