Preferred Label : t(11;17)(q23;q12-21);
NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q23) of
chromosome 11 and the long arm (q12-21) of chromosome 19. It is associated with KMT2A
(MLL) fusions, including those with MLLT6 (AF17), and acute myeloid leukemia.;
NCI Metathesaurus CUI : CL1378665;
Origin ID : C168760;
UMLS CUI : C5239095;
Semantic type(s)
- cytogenetic_abnormality_involves_chromosome
- molecular_abnormality_involves_gene
