Any acute myeloid leukemia that has the chromosomal anomaly t(11;15)(p15;q35). (A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 15q35. It results in the formation of NUP98/JARID1A fusion gene. It is associated with the development of acute myeloid leukemia with t(11;15)(p15;q35); NUP98-JARID1A.). The disease is Monarch Disease Ontology id MONDO_0100407 (acute myeloid leukemia, t(11;15)(p15;q35)). Also known as: AML, t(11;15)(p15;q35).