t(11;17) - CISMeF

Preferred Label : t(11;17);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 11 and 17.;

NCI Metathesaurus CUI : CL1412947;

Details

Origin ID

C175582;

UMLS CUI

C5446636;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 17 [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