CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Hemopexin measurement ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0523688
Disease: Hemopexin measurement
Hemopexin measurement 		0.100 GeneticVariation phenotype GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269 2017