F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency 		0.800 Biomarker disease CTD_human
CUI: C4722227
Disease: Hypoprothrombinemias
Hypoprothrombinemias 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.500 Biomarker group HPO
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.500 Biomarker disease HPO
CUI: C0272317
Disease: Hereditary factor II deficiency disease
Hereditary factor II deficiency disease 		0.500 SusceptibilityMutation disease CLINVAR
CUI: C0272317
Disease: Hereditary factor II deficiency disease
Hereditary factor II deficiency disease 		0.500 CausalMutation disease CLINVAR
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		0.420 Biomarker phenotype HPO
CUI: C3160733
Disease: THROMBOPHILIA DUE TO THROMBIN DEFECT
THROMBOPHILIA DUE TO THROMBIN DEFECT 		0.400 Biomarker phenotype GENOMICS_ENGLAND
CUI: C3280672
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2 		0.400 Biomarker disease CTD_human
CUI: C3280672
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2 		0.400 SusceptibilityMutation disease CLINVAR
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		0.350 Biomarker disease CTD_human
CUI: C0751010
Disease: Cerebral Infarction, Left Hemisphere
Cerebral Infarction, Left Hemisphere 		0.300 Biomarker phenotype CTD_human
CUI: C0751011
Disease: Cerebral Infarction, Right Hemisphere
Cerebral Infarction, Right Hemisphere 		0.300 Biomarker phenotype CTD_human
CUI: C0751012
Disease: Anterior Choroidal Artery Infarction
Anterior Choroidal Artery Infarction 		0.300 Biomarker phenotype CTD_human
CUI: C0751014
Disease: Subcortical Infarction
Subcortical Infarction 		0.300 Biomarker disease CTD_human
CUI: C0887799
Disease: Posterior Choroidal Artery Infarction
Posterior Choroidal Artery Infarction 		0.300 Biomarker phenotype CTD_human
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		0.200 Biomarker disease HPO
CUI: C0002871
Disease: Anemia
Anemia 		0.120 Biomarker disease HPO
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		0.100 Biomarker phenotype HPO
CUI: C0013491
Disease: Ecchymosis
Ecchymosis 		0.100 Biomarker phenotype HPO
CUI: C0014591
Disease: Epistaxis
Epistaxis 		0.100 Biomarker phenotype HPO
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage 		0.100 Biomarker phenotype HPO
CUI: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage 		0.100 Biomarker phenotype HPO
CUI: C0018924
Disease: Hemarthrosis
Hemarthrosis 		0.100 Biomarker phenotype HPO