t(11;19)(q23;p13)

Preferred Label : t(11;19)(q23;p13);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT1 (ENL) and ELL, and acute myeloid leukemia.;

NCI Metathesaurus CUI : CL358800;

Détails

Origin ID

C168764;

UMLS CUI

C5239098;

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 11 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]

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

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