B-cell acute lymphoblastic leukemia B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) https://www.malacards.org/card/b_lymphoblastic_leukemia_lymphoma_with_t119q23p133 https://www.malacards.org/card/b_lymphoblastic_leukemia_lymphoma_with_tcf3_pbx1 UMLS:C2698315 DOID:0080649 B lymphoblastic leukaemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) (morphologic abnormality) B-acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) B lymphoblastic leukemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) (morphologic abnormality) 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. GARD:0022348 B-acute lymphoblastic leukaemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3) MEDGEN:396324 SCTID:450956008 B acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) MONDO:0600030 NCIT:C80347 Orphanet:585956 B acute lymphoblastic leukaemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)