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t(6;9)(p22.3;q34.1)

MedGen UID:
308382
•Concept ID:
C1515781
•
Cell or Molecular Dysfunction
Synonyms: t(6;9)(p22;q34); t(6;9)(p23;q34); t(6;9)(p23;q34.1)

Definition

A cytogenetic abnormality that refers to the translocation of the short arm (p22.3) of chromosome 6 and the long arm (q34.1) of chromosome 9. It is associated with DEK/NUP214 fusions, acute myeloid leukemia and myelodysplastic syndromes. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(6;9)(p22.3;q34.1)

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