Acute myeloid leukemia, t(v;11q23.3)

MONDO:0100386

Any acute myeloid leukemia that has the chromosomal anomaly t(v;11q23.3). (A chromosomal abnormality consisting of the translocation of genetic material from any one of several chromosomes to the 11q23.3 region, resulting in an MLL gene rearrangement.)

Also known as: AML, 11q23.3 Translocation, AML, t(11;v)(q23.3;v), AML, t(11;v)(q23;v), AML, t(V;11)(v;q23), AML, t(V;11)(v;q23.3), AML, t(v;11q23.3)

2855 clinical trials for this condition and its sub-types.

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