Disease Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0.800 GeneticVariation UNIPROT Molecular determinants of α-synuclein mutants' oligomerization and membrane interactions. 25561023 2015
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0.800 CausalMutation CLINVAR Yeast reveal a "druggable" Rsp5/Nedd4 network that ameliorates α-synuclein toxicity in neurons. 24158909 2013
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0.800 CausalMutation CLINVAR Identification and rescue of α-synuclein toxicity in Parkinson patient-derived neurons. 24158904 2013
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0.800 CausalMutation CLINVAR First appraisal of brain pathology owing to A30P mutant alpha-synuclein. 20437567 2010
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0.800 CausalMutation CLINVAR Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers. 11376188 2001
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0.800 GeneticVariation UNIPROT Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. 9462735 1998
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
0.800 CausalMutation CLINVAR Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. 9462735 1998