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.;

Détails

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]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients