t(17;19)(q22;p13)

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

NCIt synonyms : t 17 19 q22 p13;

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]