Parkinson Disease 20, Early-Onset

Preferred Label : Parkinson Disease 20, Early-Onset;

NCIt synonyms : PARK20;

NCIt definition : An autosomal recessive subtype of Parkinson disease, caused by mutation(s) in the SYNJ1 gene, encoding synaptojanin-1.;

Details

Origin ID

C203535;

UMLS CUI

C3809824;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Parkinson disease 20, early-onset [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- SYNJ1 Gene [NCIt concept]

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