" /> t(11;15)(p15;q35) - CISMeF





Preferred Label : t(11;15)(p15;q35);

NCIt definition : 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.;

NCI Metathesaurus CUI : CL514689;

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04/05/2025


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