Parkinsonism with Polyneuropathy

Preferred Label : Parkinsonism with Polyneuropathy;

NCIt synonyms : PKNPY;

NCIt definition : An autosomal dominant subtype of Parkinson disease, caused by mutation(s) in the UQCRC1 gene, encoding cytochrome b-c1 complex subunit 1, mitochondrial.;

NCI Metathesaurus CUI : CL1767179;

Details

Origin ID

C201521;

UMLS CUI

C5543299;

Currated CISMeF NLP mapping
- Parkinsonism with polyneuropathy [OMIM Phenotype]
- Parkinsonism with polyneuropathy [ORDO Disease]
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)
- Parkinsonism with polyneuropathy [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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