t(4;14)(p16;q32)

Preferred Label : t(4;14)(p16;q32);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p16) of chromosome 4 and the long arm (q32) of chromosome 14.;

NCI Metathesaurus CUI : CL428549;

Details

Origin ID

C128658;

UMLS CUI

C4287938;

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 14 [NCIt concept]
- Human Chromosome 4 [NCIt concept]
is_abnormality_of_gene
- FGFR3/IGH Fusion Gene [NCIt concept]

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