DRD3, dopamine receptor D3, 1814

N. diseases: 199; N. variants: 13
Disease: Osteofibrous Dysplasia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1709353
Disease: Osteofibrous Dysplasia
Osteofibrous Dysplasia 		0.010 GeneticVariation disease BEFREE In a stepwise multiple regression analysis, 5-HT2C and DRD3 genotype (5-HT2Cser and DRD3gly allele carriage) respectively contributed 4.2% and 4.7% to the variance in OFD scores. 11140333 2000