t(8;21) - CISMeF

Preferred Label : t(8;21);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 8 and 21.;

Origin ID

C119608;

UMLS CUI

C3897139;

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