t(16;16) - CISMeF

Preferred Label : t(16;16);

NCIt definition : A cytogenetic abnormality that involves a translocation occurring within chromosome 16.;

NCI Metathesaurus CUI : CL509584;

Détails

Origin ID

C128645;

UMLS CUI

C4287945;

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 16 [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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