C116396Level 7
KIT Exon 17 Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A molecular genetic abnormality indicating the presence of a mutation in exon 17 of the KIT gene located within 4q11-q12.
**Synonyms:** - CD117 Exon 17 Mutation - CKIT Mutation - Ex17 - Exon 17 - KIT Proto-Oncogene Tyrosine Protein Kinase Gene Exon 17 Mutation - c-KIT Exon 17 Mutation - v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Exon 17 Mutation
GET
/api/v1/systems/nci_thesaurus/nodes/C116396Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.