Acute myeloid leukemia, t(11;19)(q23;p13)

MONDO:0100383

Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT1 (ENL) and ELL, and acute myeloid leukemia.)

Also known as: AML, t(11;19)(q23;p13)

3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(11;19)(q23;p13) itself.

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