Acute myeloid leukemia, t(11;15)(p15;q35)

MONDO:0100407

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.)

Also known as: AML, t(11;15)(p15;q35)

3091 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, t(11;15)(p15;q35) itself.

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Including sub-types (3091) Tagged with Acute myeloid leukemia, t(11;15)(p15;q35) (0)

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