t(11;17)(q23;q12-21)

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;

Détails

Origin ID

C168760;

UMLS CUI

C5239095;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 17 [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]
- KMT2A/MLLT6 Fusion Gene [NCIt concept]
- MLLT6 Gene [NCIt concept]

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