U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

DDX41-Related Predisposition to Leukemia

MedGen UID:
1791436
•Concept ID:
C5554995
•
Finding

Definition

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

Supplemental Content

Table of contents

    Practice guidelines

    • Bookshelf
      See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...