t(15;17) - CISMeF

Preferred Label : t(15;17);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 15 and 17.;

NCI Metathesaurus CUI : CL509583;

Détails

Origin ID

C128656;

UMLS CUI

C4287946;

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]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 15 [NCIt concept]
- Human Chromosome 17 [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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