t(17;19)(q22;p13)

Preferred Label : t(17;19)(q22;p13);

NCIt synonyms : t 17 19 q22 p13;

NCIt definition : A chromosomal translocation involving breakpoints within the q22 band on the long arm of chromosome 17 and the p13 band on the short arm of chromosome 19. This rearrangement is associated with TCF3-HLF fusion gene expression and acute lymphoblastic leukemia.;

Details

Origin ID

C36361;

UMLS CUI

C1515729;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 17 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
is_abnormality_of_gene
- TCF3/HLF Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- HLF Gene [NCIt concept]
- TCF3 Gene [NCIt concept]
- TCF3/HLF Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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