t(9;22)(q22;q12)

Preferred Label : t(9;22)(q22;q12);

NCIt definition : A chromosomal translocation involving the NR4A3 gene at 9q22 and the EWSR1 gene at 22q12.;

NCI Metathesaurus CUI : CL1411990;

Détails

Origin ID

C174484;

UMLS CUI

C5420802;

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 22 [NCIt concept]
- Human Chromosome 9 [NCIt concept]
is_abnormality_of_gene
- EWSR1/NR4A3 Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- EWSR1 Gene [NCIt concept]
- EWSR1/NR4A3 Fusion Gene [NCIt concept]
- FET Family Gene [NCIt concept]
- NR4A3 Gene [NCIt concept]

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

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