Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0019065
Disease: Hemoperitoneum
Hemoperitoneum 		1 0 1 0.17 0 0
CUI: C0266785
Disease: Abnormal umbilical cord
Abnormal umbilical cord 		1 0 1 0.17 0 0
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		1 0 1 0.17 0 0
CUI: C0269608
Disease: Antepartum hemorrhage
Antepartum hemorrhage 		1 0 1 0.17 0 0
CUI: C0270027
Disease: Antepartum hemorrhage affecting fetus or newborn
Antepartum hemorrhage affecting fetus or newborn 		1 0 1 0.17 0 0
CUI: C0272327
Disease: Hereditary factor X deficiency disease
Hereditary factor X deficiency disease 		1 0 1 0.17 0 0
CUI: C0339815
Disease: Anterior epistaxis
Anterior epistaxis 		1 0 1 0.17 0 0
CUI: C0584983
Disease: Homozygous Factor V Leiden mutation
Homozygous Factor V Leiden mutation 		1 0 1 0.17 0 0
CUI: C0749098
Disease: Hematoma, Subdural, Acute
Hematoma, Subdural, Acute 		1 0 1 0.17 0 0
CUI: C0751797
Disease: Intracranial Hematoma, Traumatic
Intracranial Hematoma, Traumatic 		1 0 1 0.17 0 0
CUI: C1142442
Disease: Intrahepatic biloma
Intrahepatic biloma 		1 0 1 0.17 0 0
CUI: C2750481
Disease: Factor XIII, B Subunit, Deficiency Of
Factor XIII, B Subunit, Deficiency Of 		1 0 1 0.17 0 0
CUI: C2750514
Disease: Factor Xiii, A Subunit, Deficiency Of
Factor Xiii, A Subunit, Deficiency Of 		1 0 1 0.17 0 0
CUI: C2873787
Disease: Deficiency of factor X [Stuart-Prower]
Deficiency of factor X [Stuart-Prower] 		1 0 1 0.17 0 0
CUI: C3203356
Disease: Factor II deficiency
Factor II deficiency 		1 0 1 0.17 0 0
CUI: C3280672
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2 		1 0 1 0.17 0 0
CUI: C3890031
Disease: prothrombin type 3 phenotype
prothrombin type 3 phenotype 		1 0 1 0.17 0 0
CUI: C4016042
Disease: VENOUS THROMBOSIS, SUSCEPTIBILITY TO
VENOUS THROMBOSIS, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C4016343
Disease: DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II
DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II 		1 0 1 0.17 0 0
CUI: C4021097
Disease: Reduced prothrombin activity
Reduced prothrombin activity 		1 0 1 0.17 0 0
CUI: C4293689
Disease: Abnormal proerythroblast morphology
Abnormal proerythroblast morphology 		1 0 1 0.17 0 0
CUI: C4722227
Disease: Hypoprothrombinemias
Hypoprothrombinemias 		1 0 1 0.17 0 0
CUI: C0019195
Disease: Hepatitis, Viral, Human
Hepatitis, Viral, Human 		2 0 1 0.14 0 0
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency 		2 0 2 0.33 0 0
CUI: C0259744
Disease: dysproteinemia
dysproteinemia 		2 0 1 0.14 0 0