Acute myeloid leukemia, t(11;19)(q23;p13.1)

MONDO:0100384

Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13.1). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13.1) of chromosome 19. It is associated with the development of acute myeloid leukemia with variant MLL translocations and topoisomerase II inhibitor-related acute myeloid leukemia.)

Also known as: AML, t(11;19)(q23;p13.1)

3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(11;19)(q23;p13.1) itself.

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↑ Acute myeloid leukemia (1192)

Including sub-types (3080) Tagged with Acute myeloid leukemia, t(11;19)(q23;p13.1) (0)

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