acute myeloid leukemia, t(5;11)(q35;p15) (MONDO_0100395, a Monarch Disease Ontology identifier) is any acute myeloid leukemia that has the chromosomal anomaly t(5;11)(q35;p15). (A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 5q35. It results in the formation of NUP98/NSD1 fusion gene. It is associated with the development of acute myeloid leukemia with t(5;11)(q35;p15); NUP98-NSD1.). Also known as: AML, t(5;11)(q35;p15).