Acute myeloid leukemia, t(15;17)(q24;q21)

From BugSigDB


Any acute myeloid leukemia that has the chromosomal anomaly t(15;17)(q24;q21). (A chromosomal translocation associated with creation of a fusion between the PML and RARA genes. It is seen in variants of acute promyelocytic leukemia.)
Aliases
  • AML, t(15;17)(q22;q12)
  • AML, t(15;17)(q22;q21)
  • AML, t(15;17)(q24;q21)