Acute myeloid leukemia, t(10;11)(p11.2;q23)

MONDO:0100378

Any acute myeloid leukemia that has the chromosomal anomaly t(10;11)(p11.2;q23). (A cytogenetic abnormality that refers to the translocation of the short arm (p11.2) of chromosome 10 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/ABI1 fusions and acute myeloid leukemia.)

Also known as: AML, t(10;11)(p11.2;q23)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(10;11)(p11.2;q23) itself.

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Including sub-types (3091) Tagged with Acute myeloid leukemia, t(10;11)(p11.2;q23) (0)

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