C39718Level 5
PDGFRA Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A molecular genetic abnormality indicating the presence of a mutation in the PDGFRA (platelet-derived growth factor receptor, alpha polypeptide) gene on chromosome 4q12.
**Synonyms:** - CD140A Gene Mutation - PDGFR-2 Gene Mutation - PDGFR2 Gene Mutation - PDGFRA Mutation - PDGFRalpha Gene Mutation - Platelet-Derived Growth Factor Receptor Alpha Gene Mutation - RHEPDGFRA Gene Mutation
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