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.)
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childhood acute myeloid leukemia
MONDO:0004996
acute monocytic leukemia
MONDO:0007896
acute promyelocytic leukemia
MONDO:0012883
acute myeloid leukemia with t(8;21)(q22;q22) translocation
MONDO:0015166
acute myeloid leukemia by FAB classification
MONDO:0015667
inherited acute myeloid leukemia
MONDO:0017893