t(11;18) - CISMeF

Preferred Label : t(11;18);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 11 and 18.;

NCI Metathesaurus CUI : CL525739;

Details

Origin ID

C138176;

UMLS CUI

C4527418;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 18 [NCIt concept]

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