acute myeloid leukemia, t(10;11)(p11.2;q23)
MONDO:0100378Mondo
Findings
No curated finding names acute myeloid leukemia, t(10;11)(p11.2;q23) 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(10;11)(p11.2;q23). (A cytogenetic abnormality that refers to the translocation of the short arm (p11.2) of chromosome 10 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/ABI1 fusions and acute myeloid leukemia.)
Definition from the Mondo Disease Ontology (MONDO:0100378), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: acute myeloid leukemia, t(10;11)(p11.2;q23)
- Also called
- AML, t(10;11)(p11.2;q23)