Acute myeloid leukemia, t(3;5)(q25;q34)

Definition

Any acute myeloid leukemia that has the chromosomal anomaly t(3;5)(q25;q34). (A cytogenetic abnormality that refers to the translocation of the long arm (q25) of chromosome 3 and the long arm (q34) of chromosome 5. It is associated with the development of acute myeloid leukemia arising from myelodysplastic syndrome, acute myeloid leukemia with multilineage dysplasia, and acute myeloid leukemia with myelodysplasia-related changes.)

Also known as AML, t(3;5)(q25;q34) — per MONDO

Also identified as

• DOID 0081092 per MONDO
• NCIT C7600 per MONDO

Affected Organs