Acute myeloid leukemia, t(10;11)(p12;q23)

MONDO:0100377

Any acute myeloid leukemia that has the chromosomal anomaly t(10;11)(p12;q23). (A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood.)

Also known as: AML, t(10;11)(p12;q23)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(10;11)(p12;q23) itself.

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↑ Acute myeloid leukemia (1194)

Including sub-types (3091) Tagged with Acute myeloid leukemia, t(10;11)(p12;q23) (0)

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