U.S. flag

An official website of the United States government


Send to:

Choose Destination


MedGen UID:
Concept ID:
Cell or Molecular Dysfunction
Synonyms: t(1;19) (q23;p13.3); PBX/E2A; t(1;19)(q23;p13.3); PBX/E2A


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. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;19)(q23;p13.3)

Supplemental Content

Table of contents

    Practice guidelines

    • Bookshelf
      See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...