acute myeloid leukemia, t(11;19)(q23;p13.1)
MONDO:0100384Mondo
Findings
No curated finding names acute myeloid leukemia, t(11;19)(q23;p13.1) 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(11;19)(q23;p13.1). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13.1) of chromosome 19. It is associated with the development of acute myeloid leukemia with variant MLL translocations and topoisomerase II inhibitor-related acute myeloid leukemia.)
Definition from the Mondo Disease Ontology (MONDO:0100384), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: acute myeloid leukemia, t(11;19)(q23;p13.1)
- Also called
- AML, t(11;19)(q23;p13.1)