DRD3, dopamine receptor D3, 1814

N. diseases: 199; N. variants: 13
Disease: Dyslexia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.010 Biomarker disease BEFREE Sequencing of two positional candidate genes, 5HT1F and DRD3, did not support their role in dyslexia. 11584043 2001