Parkinson Disease-18, Autosomal Dominant

Preferred Label : Parkinson Disease-18, Autosomal Dominant;

NCIt synonyms : PARK18;

NCIt definition : An autosomal dominant form of Parkinson disease caused by mutation(s) in the EIF4G1 gene encoding eukaryotic translation initiation factor 4 gamma 1.;

Details

Origin ID

C214869;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
disease_mapped_to_gene
- EIF4G1 Gene [NCIt concept]

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