t(2;12) - CISMeF

Preferred Label : t(2;12);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 2 and 12.;

NCI Metathesaurus CUI : CL1407502;

Details

Origin ID

C173543;

UMLS CUI

C5420255;

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 12 [NCIt concept]

Keyword's position in hierarchy(ies) :

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