Acute myeloid leukemia, t(3;3)(q21.3;q26.2)

Definition

Any acute myeloid leukemia that has the chromosomal anomaly t(3;3)(q21.3;q26.2). (A cytogenetic abnormality that refers to the translocation where both breakpoints are on the long arm (q23.1 and q26.2) of chromosome 3. It is associated with acute myeloid leukemia.)

Also known as AML, t(3;3)(q21;q26.2), AML, t(3;3)(q21.3;q26.2), AML, t(3;3)(q21.3q26.2), AML, t(3;3)(q26;q21) — per MONDO

Also identified as

• NCIT C122717 per MONDO

Affected Organs