" /> t(10;11)(p12;q23) - CISMeF





Preferred Label : t(10;11)(p12;q23);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood.;

NCI Metathesaurus CUI : CL358822;

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04/05/2025


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