t(12;22;20)(q13;q12;q11)

Preferred Label : t(12;22;20)(q13;q12;q11);

NCIt definition : A complex cytogenetic abnormality that refers to a chromosomal translocation involving the long arm (q13) of chromosome 12, the long arm (q12) of chromosome 22 and the long arm (q11) of chromosome 20. It is associated with the expression of EWSR1/DDIT3 fusions and myxoid liposarcomas.;

NCI Metathesaurus CUI : CL1906504;

Détails

Origin ID

C199596;

UMLS CUI

C5855702;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 12 [NCIt concept]
- Human Chromosome 20 [NCIt concept]
- Human Chromosome 22 [NCIt concept]
molecular_abnormality_involves_gene
- DDIT3 Gene [NCIt concept]
- EWSR1 Gene [NCIt concept]
- EWSR1/DDIT3 Fusion Gene [NCIt concept]
- FET Family Gene [NCIt concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients