acute myeloid leukemia acute myeloid leukemia, t(11;19)(q23;p13) https://github.com/monarch-initiative/mondo/issues/3452 GARD:0026167 Any acute myeloid leukemia that has the chromosomal anomaly t(11;19)(q23;p13). (A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT1 (ENL) and ELL, and acute myeloid leukemia.) MONDO:0100383 AML, t(11;19)(q23;p13)