Acute myeloid leukemia, t(6;9)(p23;q34.1)
MONDO:0100382Any acute myeloid leukemia that has the chromosomal anomaly t(6;9)(p23;q34.1). (A cytogenetic abnormality that refers to the translocation of the short arm (p23) of chromosome 6 and the long arm (q34.1) of chromosome 9. It is associated with DEK/NUP214 fusions, acute myeloid leukemia and myelodysplastic syndromes.)
Also known as: AML, t(6;9)(p22.3;q34.1), AML, t(6;9)(p22;q34), AML, t(6;9)(p23;q34), AML, t(6;9)(p23;q34.1)
3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(6;9)(p23;q34.1) itself.
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