t(1;19)(q23;p13.3)

Preferred Label : t(1;19)(q23;p13.3);

NCIt synonyms : t(1;19) (q23;p13.3); PBX/E2A; t(1;19)(q23;p13.3); PBX/E2A; t 1 19 q23 p13 3 PBX E2A;

NCIt related terms : TCF3-PBX1 t(1;19);

NCIt definition : A chromosomal abnormality consisting of the translocation of 19p13.3 with 1q23, resulting in the fusion of the TCF3 (E2A) gene with the PBX1 gene.;

Details

Origin ID

C27715;

UMLS CUI

C1515739;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
is_abnormality_of_gene
- TCF3/PBX1 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- B Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); TCF3-PBX1 [NCIt concept]
molecular_abnormality_involves_gene
- PBX1 Gene [NCIt concept]
- TCF3 Gene [NCIt concept]
- TCF3/PBX1 Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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