t(2;22)(q33.3;q12)

Preferred Label : t(2;22)(q33.3;q12);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the long arm (q33.3) of chromosome 2 and the long arm (q12) of chromosome 22.;

NCI Metathesaurus CUI : CL1906498;

Details

Origin ID

C199598;

UMLS CUI

C5855703;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 2 [NCIt concept]
- Human Chromosome 22 [NCIt concept]

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