Xp11.2 Translocation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A cytogenetic abnormality that refers to any translocation involving Xp11.2 on the short arm of the X chromosome.

**Synonyms:** - t(V;X)(v;p11.2) - t(X;V)(p11.2;v) - t(v;Xp11.2)