t(3;3) - CISMeF

Preferred Label : t(3;3);

NCIt definition : A cytogenetic abnormality that involves a translocation occurring within chromosome 3.;

NCI Metathesaurus CUI : CL509589;

Details

Origin ID

C128647;

UMLS CUI

C4287940;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CPTAC Acute Myeloid Leukemia Baseline Form [NCIt concept]
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 3 [NCIt concept]

Keyword's position in hierarchy(ies) :

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