t(8;8)(q13;q21)

Preferred Label : t(8;8)(q13;q21);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation involving 2 break points within the long arm (q13 and q21) of chromosome 8. It may be associated with the expression of CA3/MYBL1 fusions.;

NCI Metathesaurus CUI : CL1906510;

Details

Origin ID

C199601;

UMLS CUI

C5855705;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 8 [NCIt concept]
molecular_abnormality_involves_gene
- CA3 Gene [NCIt concept]
- MYBL1 Gene [NCIt concept]

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