Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5555
Gene Symbol: PRH2
PRH2
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.010 Biomarker BEFREE At present, different congenital defects in several proteins--antithrombin III (AT III), protein C (PC), protein S (PS), and plasminogen (PLG)--are known to be causes of hereditary predisposition to thrombosis (thrombophilia). 1826407

1991