Acute myeloid leukemia, t(10;11)(p12;q23)

Acute myeloid leukemia, t(10;11)(p12;q23)

Definition

Any acute myeloid leukemia that has the chromosomal anomaly t(10;11)(p12;q23). (A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood.)

Also known as AML, t(10;11)(p12;q23) — per MONDO

Also identified as

Affected Organs

Organ Involvement Source
Bone marrow Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Bone marrow Disease Has Primary Anatomic Site NCIT · CC BY 4.0