t(10;11)(p12.1;q23.3)

Preferred Label : t(10;11)(p12.1;q23.3);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p12.1) of chromosome 10 and the long arm (q23.3) of chromosome 11. It is associated with KMT2A (MLL) fusions.;

NCI Metathesaurus CUI : CL972424;

Details

Origin ID

C167197;

UMLS CUI

C5238354;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- 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]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]

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