t(9;17)(q22;q11.2)

Preferred Label : t(9;17)(q22;q11.2);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation involving the long arm (q22) of chromosome 9 and the long arm (q11.2) of chromosome 17. It may be associated with the expression of TAF15/NR4A3 fusions and extraskeletal myxoid chondrosarcoma.;

NCI Metathesaurus CUI : CL1906509;

Détails

Origin ID

C199602;

UMLS CUI

C5855706;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 17 [NCIt concept]
- Human Chromosome 9 [NCIt concept]
molecular_abnormality_involves_gene
- FET Family Gene [NCIt concept]
- NR4A3 Gene [NCIt concept]
- TAF15 Gene [NCIt concept]
- TAF15/NR4A3 Fusion Gene [NCIt concept]

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

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