Acute myeloid leukemia, t(9;22)(q34.1;q11.2)

Definition

Any acute myeloid leukemia that has the chromosomal anomaly t(9;22)(q34.1;q11.2). (A translocation between chromosomes 9 and 22 that is associated with the Philadelphia chromosome.)

Also known as AML, t(9;22)(q34;q11.2), AML, t(9;22)(q34;q11), AML, t(9;22)(q34.1;q11.2) — per MONDO