t(10;11)(p11.2;q23)

Preferred Label : t(10;11)(p11.2;q23);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p11.2) of chromosome 10 and the long arm (q23) of chromosome 11. It is associated with KMT2A (MLL)/ABI1 fusions and acute myeloid leukemia.;

NCI Metathesaurus CUI : CL1378668;

Détails

Origin ID

C168758;

UMLS CUI

C5239093;

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]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 10 [NCIt concept]
- Human Chromosome 11 [NCIt concept]
molecular_abnormality_involves_gene
- ABI1 Gene [NCIt concept]
- KMT2A Gene [NCIt concept]
- MLL/ABI1 Fusion Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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