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t(9;11)(p21.3;q23.3)

MedGen UID:
271885
•Concept ID:
C1515800
•
Cell or Molecular Dysfunction
Synonym: t(9;11)(p22;q23)

Definition

A cytogenetic abnormality that refers to the translocation of the short arm (p21.3) of chromosome 9 and the long arm (q23.3) of chromosome 11. It is associated with the development of acute myeloid leukemia with the MLLT3-MLL fusion gene transcript. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(9;11)(p21.3;q23.3)

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