C136643Level 7
Non-synonymous PDGFR Family Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation in a gene that is a member of the PDGFR gene family that encodes an amino acid substitution in a PDGFR family protein.
**Synonyms:** - Non-synonymous Platelet Derived Growth Factor Receptor Family Gene Mutation - PDGFR Family Gene Missense Mutation
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