Parkinson disease 5, autosomal dominant, susceptibility to

Go to external page http://purl.obolibrary.org/obo/MONDO_0013340


Any young-onset Parkinson disease in which the cause of the disease is a mutation in the UCHL1 gene. [ MONDO:patterns/disease_series_by_gene ]

This is just here as a test because I lose it

Term information

Subsets

predisposition

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/susceptibility_by_gene.yaml

definition

Any young-onset Parkinson disease in which the cause of the disease is a mutation in the UCHL1 gene.

exactMatch

http://linkedlifedata.com/resource/umls/id/C3150899

http://identifiers.org/omim/613643

has exact synonym

young-onset Parkinson disease caused by mutation in UCHL1

Parkinson disease 5, autosomal dominant, susceptibility to

UCHL1 young-onset Parkinson disease

has related synonym

PARK5

susceptibility to autosomal dominant Parkinson disease 5

id

MONDO:0013340