Acute myeloid leukemia, t(6;11)(q27;q23)

Definition

Any acute myeloid leukemia that has the chromosomal anomaly t(6;11)(q27;q23). (A cytogenetic abnormality that refers to the translocation of the long arm (q27) of chromosome 6 and the long arm (q23) of chromosome 11. It is associated with the development of de novo acute myeloid leukemia.)

Also known as AML, t(6;11)(q27;q23.3), AML, t(6;11)(q27;q23) — per MONDO

Also identified as

• NCIT C132105 per MONDO

Affected Organs