t(3;12)(q26.2;p13.2)

Preferred Label : t(3;12)(q26.2;p13.2);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 3q26.2 with chromosome 12p13.2. It results in the expression of ETV6-MECOM fusion gene.;

NCI Metathesaurus CUI : CL1906295;

Details

Origin ID

C198848;

UMLS CUI

C5855170;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 12 [NCIt concept]
- Human Chromosome 3 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(3;12)(q26.2;p13.2); ETV6-MECOM [NCIt concept]
molecular_abnormality_involves_gene
- ETS Family Gene [NCIt concept]
- ETV6 Gene [NCIt concept]
- MECOM Gene [NCIt concept]

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