Acute myeloid leukemia, t(1;11)(q21;q23)

MONDO:0100379

Any acute myeloid leukemia that has the chromosomal anomaly t(1;11)(q21;q23). (A cytogenetic abnormality that refers to the translocation of the long arm (q21) of chromosome 1 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/MLLT11 (AF1Q) fusions, acute myeloid leukemia and some cases of acute lymphoblastic leukemia.)

Also known as: AML, t(1;11)(q21;q23)

3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(1;11)(q21;q23) itself.

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