t(17;19) - CISMeF

Preferred Label : t(17;19);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 17 and 19.;

NCI Metathesaurus CUI : CL978549;

Details

Origin ID

C165248;

UMLS CUI

C5237025;

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 17 [NCIt concept]
- Human Chromosome 19 [NCIt concept]

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