Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9456
Gene Symbol: HOMER1
HOMER1
0.300 Biomarker phenotype CTD_human Association of common genetic variants of HOMER1 gene with levodopa adverse effects in Parkinson's disease patients. 24126708 2014
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.120 GeneticVariation phenotype BEFREE Similarly, a higher degree of visual hallucinations is observed in SNCA mutations, probably owing to the more widespread accumulation. 31686421 2020
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.120 Biomarker phenotype BEFREE Insoluble α-synuclein was raised in the DLB group in both areas but not in AD either with or without visual hallucinations. 31511061 2019
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.120 Biomarker phenotype HPO
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A
0.100 Biomarker phenotype HPO
Entrez Id: 7957
Gene Symbol: EPM2A
EPM2A
0.100 Biomarker phenotype HPO
Entrez Id: 80331
Gene Symbol: DNAJC5
DNAJC5
0.100 Biomarker phenotype HPO
Entrez Id: 9896
Gene Symbol: FIG4
FIG4
0.100 Biomarker phenotype HPO
Entrez Id: 378884
Gene Symbol: NHLRC1
NHLRC1
0.100 Biomarker phenotype HPO
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
0.100 Biomarker phenotype HPO
Entrez Id: 55737
Gene Symbol: VPS35
VPS35
0.100 Biomarker phenotype HPO
Entrez Id: 5498
Gene Symbol: PPOX
PPOX
0.100 Biomarker phenotype HPO
Entrez Id: 1371
Gene Symbol: CPOX
CPOX
0.100 Biomarker phenotype HPO
Entrez Id: 25793
Gene Symbol: FBXO7
FBXO7
0.100 Biomarker phenotype HPO
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
0.100 Biomarker phenotype HPO
Entrez Id: 26058
Gene Symbol: GIGYF2
GIGYF2
0.100 Biomarker phenotype HPO
Entrez Id: 54982
Gene Symbol: CLN6
CLN6
0.100 Biomarker phenotype HPO
Entrez Id: 23317
Gene Symbol: DNAJC13
DNAJC13
0.100 Biomarker phenotype HPO
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.100 Biomarker phenotype HPO
Entrez Id: 1981
Gene Symbol: EIF4G1
EIF4G1
0.100 Biomarker phenotype HPO
Entrez Id: 2629
Gene Symbol: GBA
GBA
0.100 Biomarker phenotype HPO
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.050 Biomarker phenotype BEFREE Indeed, through the first phase of the disease (2011-2014), the patient predominantly showed: extrapyramidal features, initial cognitive decline, sleep disturbances, and visual hallucinations, together with a reduced dopamine transporter uptake in basal ganglia at the DATscan, suggesting a diagnosis of DLB. 31127780 2019
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.050 Biomarker phenotype BEFREE Our results suggest that the genetic variants DRD3 and DAT1, along with other therapeutic confounders, may influence the prevalence ratio of visual hallucinations. 30794329 2019
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.050 Biomarker phenotype BEFREE Patients who developed VHs had 18.4% lower DAT binding in the right ventral striatum (P = 0.009), 16.7% lower binding in the left ventral striatum (P = 0.02) and 18.8% lower binding in the right putamen (P = 0.03) compared to patients who did not develop VHs. 28834102 2017
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.050 GeneticVariation phenotype BEFREE The authors conducted a case-control study of Parkinson's disease patients with and without visual hallucinations to investigate associations of the polymorphisms of the dopamine receptors D2 32806 C>T (Taq1A), D3 Ser9Gly and Msp1, D5 978T>C and dopamine transporter 3'-UTR 40 bp VNTR with visual hallucinations in Parkinson's disease. 14732464 2004