APOC3, apolipoprotein C3, 345

N. diseases: 153; N. variants: 15
Disease: Hypotriglyceridemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0542037
Disease: Hypotriglyceridemia
Hypotriglyceridemia 		0.110 GeneticVariation disease BEFREE Functional analysis of the missense APOC3 mutation Ala23Thr associated with human hypotriglyceridemia. 20097930 2010
CUI: C0542037
Disease: Hypotriglyceridemia
Hypotriglyceridemia 		0.110 Biomarker disease HPO