t(6;14) - CISMeF

Preferred Label : t(6;14);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 6 and 14.;

NCI Metathesaurus CUI : CL1643027;

Details

Origin ID

C177207;

UMLS CUI

C5447617;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 14 [NCIt concept]
- Human Chromosome 6 [NCIt concept]

Keyword's position in hierarchy(ies) :

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