Acute myeloid leukemia, t(2;12)
MONDO:0100391Any acute myeloid leukemia that has the chromosomal anomaly t(2;12). (A cytogenetic abnormality that involves a translocation between chromosomes 2 and 12.)
Also known as: AML, t(2;12)
3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(2;12) itself.
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