Acute myeloid leukemia, t(11;19)(q23.3;p13.3)

MONDO:0100385

Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23.3;p13.3). (A cytogenetic abnormality that refers to the translocation of the long arm (q23.3) of chromosome 11 and the short arm (p13.3) of chromosome 19. It is associated with KMT2A (MLL)/MLLT1 (ENL) fusions and acute myeloid leukemia.)

Also known as: AML, t(11;19)(q23.3;p13.3), AML, t(11;19)(q23;p13.3)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(11;19)(q23.3;p13.3) itself.

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↑ Acute myeloid leukemia (1194)

Including sub-types (3091) Tagged with Acute myeloid leukemia, t(11;19)(q23.3;p13.3) (0)

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