t(1;19)(q10;p10)

Preferred Label : t(1;19)(q10;p10);

NCIt definition : An unbalanced translocation between chromosomes 1 and 19. It is observed in oligodendrogliomas and results in the co-deletion of 1p and 19q.;

Details

Origin ID

C99418;

UMLS CUI

C3274725;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 19 [NCIt concept]

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