t(19;22)(q13;q12)

Preferred Label : t(19;22)(q13;q12);

NCIt definition : A chromosomal translocation involving the ZNF444 gene at 19q13 and the EWSR1 gene at 22q12.;

NCI Metathesaurus CUI : CL1411986;

Details

Origin ID

C174480;

UMLS CUI

C5420798;

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 19 [NCIt concept]
- Human Chromosome 22 [NCIt concept]
is_abnormality_of_gene
- EWSR1/ZNF444 Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- EWSR1 Gene [NCIt concept]
- EWSR1/ZNF444 Fusion Gene [NCIt concept]
- FET Family Gene [NCIt concept]
- ZNF444 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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