Acute myeloid leukemia, t(6;11)(q27;q23)

Any acute myeloid leukemia that has the chromosomal anomaly t(6;11)(q27;q23). (A cytogenetic abnormality that refers to the translocation of the long arm (q27) of chromosome 6 and the long arm (q23) of chromosome 11. It is associated with the development of de novo acute myeloid leukemia.)

Also known as: AML, t(6;11)(q27;q23), AML, t(6;11)(q27;q23.3)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(6;11)(q27;q23) itself.