t(1;11)(q21;q23)

Preferred Label : t(1;11)(q21;q23);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q21) of chromosome 1 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/MLLT11 (AF1Q) fusions, acute myeloid leukemia and some cases of acute lymphoblastic leukemia.;

NCI Metathesaurus CUI : CL1378667;

Details

Origin ID

C168759;

UMLS CUI

C5239094;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 11 [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]
- MLL/MLLT11 Fusion Gene [NCIt concept]
- MLLT11 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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