Acute myeloid leukemia, t(6;9)(p23;q34.1)

Definition

Any acute myeloid leukemia that has the chromosomal anomaly t(6;9)(p23;q34.1). (A cytogenetic abnormality that refers to the translocation of the short arm (p23) of chromosome 6 and the long arm (q34.1) of chromosome 9. It is associated with DEK/NUP214 fusions, acute myeloid leukemia and myelodysplastic syndromes.)

Also known as AML, t(6;9)(p22;q34), AML, t(6;9)(p22.3;q34.1), AML, t(6;9)(p23;q34.1), AML, t(6;9)(p23;q34) — per MONDO

Also identified as

• DOID 0081080 per MONDO
• NCIT C82423 per MONDO

Affected Organs