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)