LRRK2, leucine rich repeat kinase 2, 120892

N. diseases: 231; N. variants: 74
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism
0.020 GeneticVariation disease BEFREE One L444P carrier was also associated with LRRK2 G2385R variant, but no atypical Parkinsonism was observed. 21338444 2011
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism
0.020 GeneticVariation disease BEFREE Furthermore, extensive mutational screen found LRRK2 mutations to be rare among patients who presented with PSP, MSA, CBGD, and AP. 16602113 2006