Acute myeloid leukemia, t(15;17)(q24;q21)
MONDO:0100375Any 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.)
Also known as: AML, t(15;17)(q22;q12), AML, t(15;17)(q22;q21), AML, t(15;17)(q24;q21)
3091 clinical trials for this condition and its sub-types, 1 tagged with Acute myeloid leukemia, t(15;17)(q24;q21) itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of