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B Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); TCF3-PBX1

MedGen UID:
396856
•Concept ID:
C2698306
•
Neoplastic Process
Synonyms: B Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1); B Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); TCF3::PBX1; B Acute Lymphoblastic Leukemia with TCF3-PBX1 Fusion; B Acute Lymphoblastic Leukemia with TCF3::PBX1 Fusion; B-Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1); B-Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); TCF3-PBX1; B-Acute Lymphoblastic Leukemia with TCF3-PBX1 Fusion; B-Acute Lymphoblastic Leukemia with TCF3::PBX1 Fusion; B-ALL with t(1;19)(q23;p13.3); TCF3-PBX1; B-ALL with t(1;19)(q23;p13.3); TCF3::PBX1; B-Cell Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)

Definition

A B-cell acute leukemia characterized by the presence of lymphoblasts that carry a translocation between the E2A gene on chromosome 19 and the PBX1 gene on chromosome 1. It occurs in children and less often in adults. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVB Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); TCF3-PBX1

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