Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3273
Gene Symbol: HRG
HRG
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		0.130 Biomarker BEFREE Single defects comprised established causes of inherited thrombophilia: FV:Q506 (homozygous n = 10, heterozygous n = 69), protein C (homozygous n = 1; heterozygous n = 31), heterozygous type I deficiency states of protein S (n = 7), antithrombin (n = 7) and homocystinuria (n = 6); potentially inherited clotting abnormalities which may be associated with thrombophilia: F.XII (n = 3), plasminogen (n = 2), HCII (n = 1), increased HRGP (n = 4); new candidate risk factors for thrombophilia: elevated plasma levels of Lp(a) (n = 26), F.II (n = 1). 10650845

1999
Entrez Id: 3273
Gene Symbol: HRG
HRG
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		0.130 AlteredExpression BEFREE These new families confirm that genetically transmitted high levels of HRG could be associated to familial and juvenile thrombophilia. 8475479

1993
Entrez Id: 3273
Gene Symbol: HRG
HRG
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		0.130 GeneticVariation BEFREE Familial elevation of plasma histidine-rich glycoprotein in a family with thrombophilia. 3689697

1987