t(10;11)(p12;q23)

Preferred Label : t(10;11)(p12;q23);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood.;

NCI Metathesaurus CUI : CL358822;

Détails

Origin ID

C132102;

UMLS CUI

C4331805;

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 10 [NCIt concept]
- Human Chromosome 11 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-KMT2A [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]
- MLL/MLLT10 Fusion Gene [NCIt concept]
- MLLT10 Gene [NCIt concept]

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

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