t(12;13)(p13.2;q12.2)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A cytogenetic abnormality that refers to the translocation of chromosome 12p13.2 with chromosome 13q12.2. It results in ETV6-FLT3 fusion and is associated with myeloid/lymphoid neoplasms with FLT3-rearrangement.