Acute myeloid leukemia, t(3;12)(q23;p12.3)

MONDO:0100400

Any acute myeloid leukemia that has the chromosomal anomaly t(3;12)(q23;p12.3). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 3 and the short arm (p12.3) of chromosome 12. It is associated with ETV6/MECOM (EVI1) fusions, myeloproliferative disorders, myelodysplastic syndromes and acute myelogenous leukemia.)

Also known as: AML, t(3;12)(q23;p12.3)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(3;12)(q23;p12.3) itself.

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Including sub-types (3091) Tagged with Acute myeloid leukemia, t(3;12)(q23;p12.3) (0)

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