t(9;17)(q22;q11.2)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A cytogenetic abnormality that refers to a chromosomal translocation involving the long arm (q22) of chromosome 9 and the long arm (q11.2) of chromosome 17. It may be associated with the expression of TAF15/NR4A3 fusions and extraskeletal myxoid chondrosarcoma.