Acute myeloid leukemia, t(1;22)

MONDO:0100394

Any acute myeloid leukemia that has the chromosomal anomaly t(1;22). (A cytogenetic abnormality that involves a translocation between chromosomes 1 and 22.)

Also known as: AML, t(1;22)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(1;22) itself.

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