Acute myeloid leukemia, t(5;11)(q35;p15)

Acute myeloid leukemia, t(5;11)(q35;p15)

Definition

Any acute myeloid leukemia that has the chromosomal anomaly t(5;11)(q35;p15). (A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 5q35. It results in the formation of NUP98/NSD1 fusion gene. It is associated with the development of acute myeloid leukemia with t(5;11)(q35;p15); NUP98-NSD1.)

Also known as AML, t(5;11)(q35;p15) — 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