DRD1, dopamine receptor D1, 1812

N. diseases: 181; N. variants: 8
Disease: Congenital chromosomal disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.010 GeneticVariation group BEFREE The five unrelated MPPH patients neither showed submicroscopic chromosomal aberrations nor DRD1 mutations. 20503325 2010