Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
0.010 GeneticVariation BEFREE Early-onset Parkinson disease G2019S LRRK2 carriers are more likely to manifest the PIGD phenotype, which may have implications for disease course. 20008657 2009