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DDX41-Related Predisposition to Leukemia

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An autosomal dominant condition caused by mutation(s) in the DDX41 gene, encoding probable ATP-dependent RNA helicase DDX41. It is characterized by an increased risk of developing hematologic malignancies, including myeloid and lymphoid leukemias and lymphoma. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVDDX41-Related Predisposition to Leukemia

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