LPA, lipoprotein(a), 4018

N. diseases: 340; N. variants: 49
Disease: Hypolipoproteinemias ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020623
Disease: Hypolipoproteinemias
Hypolipoproteinemias 		0.300 Biomarker phenotype CTD_human Molecular basis of congenital lp(a) deficiency: a frequent apo(a) 'null' mutation in caucasians. 10484779 1999