Acute myeloid leukemia, t(5;11)(q35;p15)
MONDO:0100395Any acute myeloid leukemia that has the chromosomal anomaly t(5;11)(q35;p15). (A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 5q35. It results in the formation of NUP98/NSD1 fusion gene. It is associated with the development of acute myeloid leukemia with t(5;11)(q35;p15); NUP98-NSD1.)
Also known as: AML, t(5;11)(q35;p15)
3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(5;11)(q35;p15) itself.
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