t(1;10)(p22-31;q24-25)

Preferred Label : t(1;10)(p22-31;q24-25);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the short arm (within p22-31) of chromosome 1 and the long arm (within q24-25) of chromosome 10.;

NCI Metathesaurus CUI : CL1906503;

Details

Origin ID

C199593;

UMLS CUI

C5855699;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 10 [NCIt concept]

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