t(3;12)(q23;p12.3)

Preferred Label : t(3;12)(q23;p12.3);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 3 and the short arm (p12.3) of chromosome 12. It is associated with ETV6/MECOM (EVI1) fusions, myeloproliferative disorders, myelodysplastic syndromes and acute myelogenous leukemia.;

NCI Metathesaurus CUI : CL1378673;

Details

Origin ID

C168766;

UMLS CUI

C5239100;

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 12 [NCIt concept]
- Human Chromosome 3 [NCIt concept]
molecular_abnormality_involves_gene
- ETS Family Gene [NCIt concept]
- ETV6 Gene [NCIt concept]
- ETV6/MECOM Fusion Gene [NCIt concept]
- MECOM Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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