Parkinson Disease 17

Preferred Label : Parkinson Disease 17;

NCIt synonyms : PARK17;

NCIt definition : An autosomal dominant subtype of Parkinson disease, caused by mutation(s) in the VPS35 gene, encoding vacuolar protein sorting-associated protein 35.;

Details

Origin ID

C201520;

Currated CISMeF NLP mapping
- Parkinson disease 17 [OMIM Phenotype]
- Parkinson's disease 17 [DO Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
See also inter- (CISMeF)
- VPS35 retromer complex component [ORDO Gene]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- VPS35 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients