C136642Level 7
Non-synonymous VEGFR Family Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation in a gene that is a member of the VEGFR gene family that encodes an amino acid substitution in a VEGFR family protein.
**Synonyms:** - Non-synonymous Vascular Endothelial Growth Factor Receptor Family Gene Mutation - VEGFR Family Gene Missense Mutation
GET
/api/v1/systems/nci_thesaurus/nodes/C136642Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.