Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0087086
Disease: Thrombus
Thrombus
0.300 Biomarker phenotype CTD_human Severe congenital protein C deficiency: description of a new mutation and prophylactic protein C therapy and in vivo pharmacokinetics. 18376272 2008
CUI: C0087086
Disease: Thrombus
Thrombus
0.300 Biomarker phenotype CTD_human Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene. 11132655 2000
CUI: C0087086
Disease: Thrombus
Thrombus
0.300 Biomarker phenotype CTD_human Lipoprotein (a): its role in childhood thromboembolism. 9164807 1997
CUI: C0087086
Disease: Thrombus
Thrombus
0.300 Biomarker phenotype CTD_human Even in these risk groups, the cost-benefit ratio of selective screening is unfavorable, as today at most 70% of the hereditary thrombophilias can be diagnosed by laboratory analysis, and only very few of the patients will actually experience a thrombotic event: only 3 of 1000 carriers of APC-resistance will suffer from thrombosis during oral contraception. 8967151 1996