C222059Level 6
DDX41-Related Hematologic Tumor Predisposition Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant inherited tumor predisposition syndrome caused by germline mutations in the DDX41 gene. It is associated with an increased risk of developing hematolymphoid neoplasms.
**Synonyms:** - DDX41-Related Leukemia Predisposition
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