Acute myeloid leukemia, t(11;19)(q23;p13.1) is a type of blood cancer characterized by a specific chromosomal change. In this condition, part of chromosome 11 (at position q23) switches places with part of chromosome 19 (at position p13.1). This unusual change is linked with variant MLL translocations and has been associated with cases related to topoisomerase II inhibitor exposure. This form of leukemia causes the bone marrow to produce abnormal white blood cells. While the detailed features of the condition are still being studied, understanding the genetic abnormality helps researchers learn more about the development of acute myeloid leukemia.

Information about symptoms is currently limited for this condition.

Information about causes, genetics, and risk factors is currently limited for this condition.