t(11;19)(q23.3;p13.3)

Preferred Label : t(11;19)(q23.3;p13.3);

NCIt synonyms : t 11 19 q23 p13 3;

NCIt related terms : t(11;19)(q23;p13.3);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q23.3) of chromosome 11 and the short arm (p13.3) of chromosome 19. It is associated with KMT2A (MLL)/MLLT1 (ENL) fusions and acute myeloid leukemia.;

Détails

Origin ID

C36372;

UMLS CUI

C1515711;

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]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
is_abnormality_of_gene
- MLL/MLLT1 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(11;19)(q23.3;p13.3); KMT2A-MLLT1 [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]
- MLL/MLLT1 Fusion Gene [NCIt concept]
- MLLT1 Gene [NCIt concept]

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

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