LPA, lipoprotein(a), 4018

N. diseases: 340; N. variants: 49
Disease: Hypoalphalipoproteinemias ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		0.010 GeneticVariation disease BEFREE Apolipoprotein A-IFin. Dominantly inherited hypoalphalipoproteinemia due to a single base substitution in the apolipoprotein A-I gene. 9012641 1997