t(X;20)(p11.2;q13.3)

Preferred Label : t(X;20)(p11.2;q13.3);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the short arm (p11.2) of the X chromosome and the long arm (q13.3) of chromosome 20.;

NCI Metathesaurus CUI : CL1906506;

Détails

Origin ID

C199606;

UMLS CUI

C5855710;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 20 [NCIt concept]
- Human Chromosome X [NCIt concept]

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

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