Parkinson Disease 23, Autosomal Recessive, Early Onset

Preferred Label : Parkinson Disease 23, Autosomal Recessive, Early Onset;

NCIt synonyms : PARK23;

NCIt definition : An autosomal recessive subtype of Parkinson disease, caused by mutation(s) in the VPS13C gene, encoding intermembrane lipid transfer protein VPS13C.;

Details

Origin ID

C203536;

UMLS CUI

C4225186;

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 23, autosomal recessive early-onset [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

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