Acute myeloid leukemia, t(7;12)(q36;p13)
Acute myeloid leukemia, t(7;12)(q36;p13)
Definition
Any acute myeloid leukemia that has the chromosomal anomaly t(7;12)(q36;p13). (A chromosomal translocation involving the ETV6 gene on chromosome 12p13 and HLXB9 gene on chromosome 7q36.)
Also known as AML, t(7;12)(q36;p13) — per MONDO
Also identified as
- NCIT C122690 per MONDO
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 |