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Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA

MedGen UID:
79020
•Concept ID:
C0279641
•
Neoplastic Process
Synonyms: Childhood Acute M3 Leukemia; Childhood Acute Progranulocytic Leukemia; Childhood Acute Promyelocytic Leukemia; Childhood Acute Promyelocytic Leukemia (M3); Childhood Acute Promyelocytic Leukemia with PML-RARA; Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA Fusion; Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML::RARA; Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML::RARA Fusion; Childhood APL; Childhood M3 APL; M3 Childhood Acute Promyelocytic Leukemia; M3 Pediatric Acute Promyelocytic Leukemia; Pediatric Acute M3 Leukemia; Pediatric Acute Progranulocytic Leukemia; Pediatric Acute Promyelocytic Leukemia; Pediatric APL; Pediatric M3 APL

Definition

An acute promyelocytic leukemia with PML-RARA fusion occurring in children. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVChildhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA

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