acute myeloid leukemia, t(11;19)(q23.3;p13.3)
MONDO:0100385Mondo
Findings
No curated finding names acute myeloid leukemia, t(11;19)(q23.3;p13.3) 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(11;19)(q23.3;p13.3). (A cytogenetic abnormality that refers to the translocation of the long arm (q23.3) of chromosome 11 and the short arm (p13.3) of chromosome 19. It is associated with KMT2A (MLL)/MLLT1 (ENL) fusions and acute myeloid leukemia.)
Definition from the Mondo Disease Ontology (MONDO:0100385), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
2 names
Resolves to: acute myeloid leukemia, t(11;19)(q23.3;p13.3)
- Also called
- AML, t(11;19)(q23;p13.3)AML, t(11;19)(q23.3;p13.3)