Acute myeloid leukemia, t(16;21)(q24;q22)

MONDO:0100408

Any acute myeloid leukemia that has the chromosomal anomaly t(16;21)(q24;q22). (A cytogenetic abnormality that refers to the translocation of the long arm (q24) of chromosome 16 and the long arm (q22) of chromosome 22. It is associated with RUNX1/CBFA2T3 fusions, myelodysplastic syndromes and acute myeloid leukemia.)

Also known as: AML, t(16;21)(q24;q22)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(16;21)(q24;q22) itself.

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Including sub-types (3091) Tagged with Acute myeloid leukemia, t(16;21)(q24;q22) (0)

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