t(11;16)(q13;p11)

Preferred Label : t(11;16)(q13;p11);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the long arm (q13) of chromosome 11 and the short arm (p11) of chromosome 16.;

NCI Metathesaurus CUI : CL1906502;

Détails

Origin ID

C199594;

UMLS CUI

C5855700;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 16 [NCIt concept]

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

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