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Up to: Acute myeloid leukemia
Acute myeloid leukemia, t(15;17)(q24;q21)
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.)
This condition has no sub-types.