t(3;3)(q21.3;q26.2)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A cytogenetic abnormality that refers to the translocation where both breakpoints are on the long arm (q23.1 and q26.2) of chromosome 3. It is associated with acute myeloid leukemia.

**Synonyms:** - t(3;3)(q21.3q26.2) - t(3;3)(q21;q26.2) - t(3;3)(q21;q26.2) - t(3;3)(q26;q21)