C214869Level 10
Parkinson Disease-18, Autosomal Dominant
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant form of Parkinson disease caused by mutation(s) in the EIF4G1 gene encoding eukaryotic translation initiation factor 4 gamma 1.
**Synonyms:** - PARK18
GET
/api/v1/systems/nci_thesaurus/nodes/C214869Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.