Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
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: 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
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.050 GeneticVariation phenotype BEFREE The A9 allele of the dopamine transporter gene increases the risk of visual hallucinations during alcohol withdrawal in alcohol-dependent women. 15193761 2004
Entrez Id: 348
Gene Symbol: APOE
APOE
0.020 GeneticVariation phenotype BEFREE To determine whether the frequency of dopamine receptor genetic variants and APOE alleles in patients with PD with and without chronic visual hallucinations resembles the pattern previously documented in patients with Alzheimer disease. 11176958 2001
Entrez Id: 348
Gene Symbol: APOE
APOE
0.020 GeneticVariation phenotype BEFREE Nondemented PD patients with the APOE epsilon 4 allele have a high risk of developing drug-induced visual hallucinations. 10442253 1999
Entrez Id: 1815
Gene Symbol: DRD4
DRD4
0.010 GeneticVariation phenotype BEFREE Moreover, patients with DRD1-48 GG and 62TT genotype displayed shorter time to VHs, whereas a longer time to VHs was found in subjects carrying the DRD4 CG alleles. 27497990 2016
Entrez Id: 2896
Gene Symbol: GRN
GRN
0.010 GeneticVariation phenotype BEFREE The clinical phenotype of PGRN mutation carriers was particular because of the wide range in onset age and the frequent occurrence of early apraxia (50%), visual hallucinations (30%), and parkinsonism (30%) during the course of the disease. 17436289 2007
Entrez Id: 1812
Gene Symbol: DRD1
DRD1
0.010 GeneticVariation phenotype BEFREE Moreover, patients with DRD1-48 GG and 62TT genotype displayed shorter time to VHs, whereas a longer time to VHs was found in subjects carrying the DRD4 CG alleles. 27497990 2016
Entrez Id: 84896
Gene Symbol: ATAD1
ATAD1
0.010 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
Entrez Id: 885
Gene Symbol: CCK
CCK
0.010 GeneticVariation phenotype BEFREE These results suggest that, in Chinese, visual hallucinations in Parkinson's disease are associated with cholecystokinin -45C>T polymorphism, and this association was still observed in the presence of the cholecystokinin-A receptor TC/CC genotype, indicating a possible interaction of these two genes in the visual hallucinogenesis in Parkinson's disease. 12777967 2003
Entrez Id: 7054
Gene Symbol: TH
TH
0.010 GeneticVariation phenotype BEFREE The genotype of the TH tetranucleotide polymorphism was assessed in 204 German controls and 311 German alcohol-dependent subjects, including 63 alcoholics with a history of visual hallucinations during withdrawal delirium. 9564682 1998
Entrez Id: 5309
Gene Symbol: PITX3
PITX3
0.010 GeneticVariation phenotype BEFREE Furthermore, the PITX3 C allele carriers with PD had a poorer cognitive performance in the visuospatial domain (p<0.001) and a higher incidence of visual hallucinations. 28991698 2017
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 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