t(14;18) - CISMeF

Preferred Label : t(14;18);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 14 and 18.;

NCI Metathesaurus CUI : CL509582;

Details

Origin ID

C128643;

UMLS CUI

C4287947;

Currated CISMeF NLP mapping
- t(14;18) [EMDN type]
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 14 [NCIt concept]
- Human Chromosome 18 [NCIt concept]

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