A B-lymphoblastic leukemia/lymphoma that is characterized by the presence of lymphoblasts that carry a translocation between the TEL gene on chromosome 12 and the AML1 gene on chromosome 21, (p13.2;q22.1). It results in the production of the TEL-AML1 (ETV6-RUNX1) fusion protein.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)
MONDO:0600030
B-lymphoblastic leukemia/lymphoma MLL rearranged
MONDO:0850156
B-lymphoblastic leukemia/lymphoma with IL3-IGH
MONDO:0850160
B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like
MONDO:0850161
B-lymphoblastic leukemia/lymphoma with IAMP21
MONDO:0850162
B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)
MONDO:0957427