t(4;19)(q25;q13)

Preferred Label : t(4;19)(q25;q13);

NCIt definition : A chromosomal translocation involving the CIC gene at 19q13 and a second breakpoint on the long arm of chromosome 4 (4q25).;

NCI Metathesaurus CUI : CL1411992;

Details

Origin ID

C174482;

UMLS CUI

C5420800;

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 4 [NCIt concept]
molecular_abnormality_involves_gene
- CIC Gene [NCIt concept]

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