Acute myeloid leukemia with t(6;9)(p23;q34.1) is a type of blood cancer that involves specific changes in the chromosomes. This condition is defined by the presence of a chromosomal anomaly where the short arm of chromosome 6 at band p23 is translocated with the long arm of chromosome 9 at band q34.1. This genetic change is associated with DEK/NUP214 fusions, and it can be seen in both acute myeloid leukemia (AML) and myelodysplastic syndromes. This rare subtype of AML is identified by its unique genetic characteristics. Knowledge about the clinical aspects, patient symptoms, treatment options, and long-term outlook is still developing. Ongoing research is important to improve understanding and management of this condition.

Information about symptoms is currently limited for this condition.

Information about causes is currently limited for this condition.