t(1;22)(q23;q12)

Preferred Label : t(1;22)(q23;q12);

NCIt definition : A chromosomal translocation involving the PBX1 gene at 1q23 and the EWSR1 gene at 22q12.;

NCI Metathesaurus CUI : CL1411997;

PubMed : 25706482;

Détails

Origin ID

C174477;

UMLS CUI

C5420795;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- EWS Authorized Value Terminology [NCIt concept]
- EWS Molecular Analysis Table [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 22 [NCIt concept]
is_abnormality_of_gene
- EWSR1/PBX1 Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- EWSR1 Gene [NCIt concept]
- EWSR1/PBX1 Fusion Gene [NCIt concept]
- FET Family Gene [NCIt concept]
- PBX1 Gene [NCIt concept]

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

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