Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.330 GeneticVariation group BEFREE These results suggest that the contribution of these DRD2 gene variants in the vulnerability of antipsychotic-induced MD takes place in a more general or pleiotropic way. 21750899 2012
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.330 GeneticVariation group BEFREE Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families. 12402271 2002
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.330 GeneticVariation group BEFREE Further, DRD2 variants have been implicated in Parkinson's disease (PD) and in iatrogenically-induced movement disorders, as well as in certain migraineurs. 11256581 2000
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.330 Biomarker group CTD_human Abnormal involuntary movements: a study of dopaminergic receptor interaction. 6858777 1983