Acute myeloid leukemia, t(6;9)(p23;q34.1)

From BugSigDB


Any acute myeloid leukemia that has the chromosomal anomaly t(6;9)(p23;q34.1). (A cytogenetic abnormality that refers to the translocation of the short arm (p23) 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.)
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Aliases
  • AML, t(6;9)(p22.3;q34.1)
  • AML, t(6;9)(p22;q34)
  • AML, t(6;9)(p23;q34)
  • AML, t(6;9)(p23;q34.1)
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