t(5;18)(q35;q11)

Preferred Label : t(5;18)(q35;q11);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the long arm (q35) of chromosome 5 and the long arm (q11) of chromosome 18.;

NCI Metathesaurus CUI : CL1906500;

Details

Origin ID

C199600;

UMLS CUI

C5855704;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 18 [NCIt concept]
- Human Chromosome 5 [NCIt concept]

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