acute myeloid leukemia, t(9;11)(p21.3;q23.3)
MONDO:0100376Mondo
Findings
No curated finding names acute myeloid leukemia, t(9;11)(p21.3;q23.3) yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any acute myeloid leukemia that has the chromosomal anomaly t(9;11)(p21.3;q23.3). (A cytogenetic abnormality that refers to the translocation of the short arm (p21.3) of chromosome 9 and the long arm (q23.3) of chromosome 11. It is associated with the development of acute myeloid leukemia with the MLLT3-MLL fusion gene transcript.)
Definition from the Mondo Disease Ontology (MONDO:0100376), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
2 names
Resolves to: acute myeloid leukemia, t(9;11)(p21.3;q23.3)
- Also called
- AML, t(9;11)(p21.3;q23.3)AML, t(9;11)(p22;q23)