t(9;22)(q22-23;q11-12)

Preferred Label : t(9;22)(q22-23;q11-12);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the long arm (within q22-23) of chromosome 9 and the long arm (within q11-12) of chromosome 22.;

NCI Metathesaurus CUI : CL1906512;

Détails

Origin ID

C199603;

UMLS CUI

C5855707;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 22 [NCIt concept]
- Human Chromosome 9 [NCIt concept]

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

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