C116399Level 6
PDGFRA Exon 18 Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A molecular genetic abnormality indicating the presence of a mutation in exon 18 of the PDGFRA gene located within 4q11-q13.
**Synonyms:** - CD140A Exon 18 Mutation - Exon 18 - PDGFR-2 Exon 18 Mutation - PDGFR2 Exon 18 Mutation - RHEPDGFRA Exon 18 Mutation
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