Acute myeloid leukemia, t(10;11)(p12;q23)

From BugSigDB


Any acute myeloid leukemia that has the chromosomal anomaly t(10;11)(p12;q23). (A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood.)
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Aliases
  • AML, t(10;11)(p12;q23)
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