CHDH, choline dehydrogenase, 55349

N. diseases: 158; N. variants: 11
Disease: Hashimoto Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.010 GeneticVariation disease BEFREE Compared to controls, the frequency of the eNOSG894T (T allele) was higher in CHD (P=0.03) and Fabry (P=0.01), while the eNOS4b/a (a allele) in CHD (P=0.01) and HT patients (P=0.01). 15784171 2005