HP, haptoglobin, 3240

N. diseases: 464; N. variants: 9
Disease: Proteinuria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0033687
Disease: Proteinuria
Proteinuria 		0.010 GeneticVariation phenotype LHGDN Haptoglobin polymorphism in patients with preeclampsia. 16879055 2006