t(2;5) - CISMeF

Preferred Label : t(2;5);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 2 and 5.;

NCI Metathesaurus CUI : CL525737;

Details

Origin ID

C138175;

UMLS CUI

C4522295;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 2 [NCIt concept]
- Human Chromosome 5 [NCIt concept]

Keyword's position in hierarchy(ies) :

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