HP, haptoglobin, 3240

N. diseases: 464; N. variants: 9
Disease: Convulsive disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0234972
Disease: Convulsive disorder
Convulsive disorder 		0.010 GeneticVariation disease BEFREE Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism. 15490286 2004