t(X;22)(p11;q13)

Preferred Label : t(X;22)(p11;q13);

NCIt definition : A chromosomal translocation involving the BCOR gene at Xp11 and the ZC3H7B gene at 22q13.;

NCI Metathesaurus CUI : CL1412030;

Détails

Origin ID

C174495;

UMLS CUI

C5420810;

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 X [NCIt concept]
molecular_abnormality_involves_gene
- BCOR Gene [NCIt concept]
- ZC3H7B Gene [NCIt concept]
- ZC3H7B/BCOR Fusion Gene [NCIt concept]

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

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