Acute myeloid leukemia, t(2;12)

MONDO:0100391

Any 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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↑ Acute myeloid leukemia (1194)

Including sub-types (3091) Tagged with Acute myeloid leukemia, t(2;12) (0)

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