t(2;8) - CISMeF

Preferred Label : t(2;8);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 2 and 8.;

NCI Metathesaurus CUI : CL514690;

Details

Origin ID

C131808;

UMLS CUI

C4318493;

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 2 [NCIt concept]
- Human Chromosome 8 [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients