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Increased risk of acute myeloid leukemia, particularly associated with R882 mutations

MedGen UID:: 1686163
•Concept ID:: C5232840
•: Finding

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVIncreased risk of acute myeloid leukemia, particularly associated with R882 mutations

Pathological Conditions, Signs and Symptoms
- Pathological process
  - Disease
    - Neoplasm
      - Increased risk of acute myeloid leukemia, particularly associated with R882 mutations

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