t(16;21)(q24;q22)

Preferred Label : t(16;21)(q24;q22);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q24) of chromosome 16 and the long arm (q22) of chromosome 22. It is associated with RUNX1/CBFA2T3 fusions, myelodysplastic syndromes and acute myeloid leukemia.;

NCI Metathesaurus CUI : CL1378682;

Details

Origin ID

C168773;

UMLS CUI

C5239107;

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 16 [NCIt concept]
- Human Chromosome 21 [NCIt concept]
molecular_abnormality_involves_gene
- CBFA2T3 Gene [NCIt concept]
- RUNX1 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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