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

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

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

NCI Metathesaurus CUI : CL972421;

Details

Origin ID

C167196;

UMLS CUI

C5238353;

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]

Keyword's position in hierarchy(ies) :

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