PDYN, prodynorphin, 5173

N. diseases: 197; N. variants: 13
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation disease BEFREE Therefore, functional allelic variants in the PDYN promoter might modify the risk to develop TLE in subjects with familial predisposition. 18334734 2008