Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 Biomarker MGD

Entrez Id: 7019
Gene Symbol: TFAM
TFAM
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.300 Biomarker MGD

Entrez Id: 56652
Gene Symbol: TWNK
TWNK
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.240 Biomarker MGD

Entrez Id: 10533
Gene Symbol: ATG7
ATG7
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.230 Biomarker MGD

Entrez Id: 54700
Gene Symbol: RRN3
RRN3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.200 Biomarker MGD

Entrez Id: 1352
Gene Symbol: COX10
COX10
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.200 Biomarker MGD

Entrez Id: 10188
Gene Symbol: TNK2
TNK2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 GeneticVariation CLINVAR

Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 GeneticVariation BEFREE The possible association of 7 HLA specificities in the HLA-A locus and 16 specificities in the HLA-B locus with susceptibility to Parkinsonian syndrome was investigated in a total of 36 patients with paralysis agitans (PA), as well as in 11 patients with other Parkinsonian syndromes, and 176 controls in Japan. 7148400

1982

Entrez Id: 3105
Gene Symbol: HLA-A
HLA-A
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 GeneticVariation BEFREE There was no clear association between HLA-A or -B locus antigens and PA or other Parkinsonian syndromes. 7148400

1982

Entrez Id: 1312
Gene Symbol: COMT
COMT
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.100 AlteredExpression BEFREE The possible association of the clinical differences in L-dopa tolerance and response between Filipinos and Caucasians with Parkinson's disease, with the racial differences in RBC-COMT activity is discussed. 6734032

1984

Entrez Id: 720
Gene Symbol: C4A
C4A
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 GeneticVariation BEFREE HLA-linked complement markers in Alzheimer's and Parkinson's disease: C4 variant (C4B2) a possible marker for senile dementia of the Alzheimer type. 6538270

1984

Entrez Id: 721
Gene Symbol: C4B
C4B
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 GeneticVariation BEFREE HLA-linked complement markers in Alzheimer's and Parkinson's disease: C4 variant (C4B2) a possible marker for senile dementia of the Alzheimer type. 6538270

1984

Entrez Id: 100293534
Gene Symbol: C4B_2
C4B_2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 GeneticVariation BEFREE HLA-linked complement markers in Alzheimer's and Parkinson's disease: C4 variant (C4B2) a possible marker for senile dementia of the Alzheimer type. 6538270

1984

Entrez Id: 629
Gene Symbol: CFB
CFB
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 GeneticVariation BEFREE In senile dementia of the Alzheimer type and in Parkinson's disease, no significant difference was found in the gene frequencies of alleles at either the BF, C2, or GLO-I locus compared with those of age-matched controls. 6538270

1984

Entrez Id: 1644
Gene Symbol: DDC
DDC
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Therapeutic CTD_human Thirteen patients with idiopathic Parkinson's disease and "on-off" fluctuations on oral levodopa plus dopa decarboxylase inhibitor (DDI) were treated with continuous (24 hour) subcutaneous lisuride infusions together with a reduced dose of levodopa (plus DDI). 2969953

1988

Entrez Id: 7054
Gene Symbol: TH
TH
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker RGD Grafting fibroblasts genetically modified to produce L-dopa in a rat model of Parkinson disease. 2573072

1989

Entrez Id: 7054
Gene Symbol: TH
TH
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker BEFREE Decreased tyrosine hydroxylase messenger RNA in the surviving dopamine neurons of the substantia nigra in Parkinson's disease: an in situ hybridization study. 1979431

1990

Entrez Id: 793
Gene Symbol: CALB1
CALB1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.080 GeneticVariation BEFREE Comparison of diseased human brain tissue with age- and sex-matched controls yielded significant decreases (60-88%) in calbindin protein and mRNA in the substantia nigra (Parkinson disease), in the corpus striatum (Huntington disease), in the nucleus basalis (Alzheimer disease), and in the hippocampus and nucleus raphe dorsalis (Parkinson, Huntington, and Alzheimer diseases) but not in the cerebellum, neocortex, amygdala, or locus ceruleus. 2140897

1990

Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.400 GeneticVariation BEFREE The frequency of fifteen genotypes of CYP2D6 (debrisoquine 4-hydroxylase) in 53 patients with Parkinson's disease was determined by the polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analyses and compared with the findings in 72 healthy controls. 1349052

1992

Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.400 GeneticVariation BEFREE Individuals with a metabolic defect in the cytochrome P450 CYP2D6-debrisoquine hydroxylase gene with the poor metaboliser phenotype had a 2.54-fold (95% Cl 1.51-4.28) increased risk of Parkinson's disease. 1350805

1992

Entrez Id: 7054
Gene Symbol: TH
TH
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker BEFREE The data suggest that, in PD: (1) TH protein content is decreased in the surviving nigral dopaminergic neurons, most likely as a result of a lowered TH mRNA cellular content. 8098254

1993

Entrez Id: 4129
Gene Symbol: MAOB
MAOB
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation BEFREE The presence of MAO-B allele 1 is associated with a relative risk for PD of 2.03-fold (confidence interval, 1.44-2.61; p < 0.02). 8489207

1993

Entrez Id: 6647
Gene Symbol: SOD1
SOD1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.400 GeneticVariation BEFREE The finding of SOD variants in FALS is consistent with the hypothesis that free radicals contribute to the pathogenesis of FALS, and possibly to the pathogenesis of other neurodegenerative disorders such as Parkinson's disease, in which there is substantial evidence of oxidant stress. 7507613

1993

Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.400 GeneticVariation BEFREE These results suggest that the HhaI polymorphism in the CYP2D6 gene is a part of the molecular basis of Parkinson's disease. 7903297

1993

Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.400 GeneticVariation BEFREE Variant cytochrome P450 CYP2D6 allelic frequencies in Parkinson's disease. 8291573

1993