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

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

Definition

Any acute myeloid leukemia that has the chromosomal anomaly inv(3)(q21.3;q26.2). (A cytogenetic abnormality that refers to a paracentric inversion involving breakpoints on the long (q23.1 and q26.2) of chromosome 3. It is associated with acute myeloid leukemia.)

Also known as AML, inv(3)(q21.3;q26.2), AML, inv(3)(q21.3q26.2), AML, inv(3)(q21q26.2) — 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