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

MONDO:0100375

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.)

Also known as: AML, t(15;17)(q22;q12), AML, t(15;17)(q22;q21), AML, t(15;17)(q24;q21)

2854 clinical trials for this condition and its sub-types.

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