t(11;19)(q13;q13.4)

Preferred Label : t(11;19)(q13;q13.4);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the long arm (q13) of chromosome 11 and the long arm (q13.4) of chromosome 19. It may be associated with the expression of MALAT1 gene rearrangement and undifferentiated embryonal sarcoma arising in mesenchymal hamartoma of the liver.;

NCI Metathesaurus CUI : CL1906505;

PubMed : 17311249;

Details

Origin ID

C199595;

UMLS CUI

C5855701;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
molecular_abnormality_involves_gene
- MALAT1 Gene [NCIt concept]

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