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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic
0 1 0 0 1 1.8E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.8E-02
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion
0 1 0 0 1 1.8E-02
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency
0 1 0 0 1 1.8E-02
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood
0 20 0 0 1 1.3E-02
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial
0 5 0 0 1 1.7E-02
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease
0 78 0 0 1 7.5E-03
CUI: C0221065
Disease: Subacute Combined Degeneration
Subacute Combined Degeneration
0 1 0 0 1 1.8E-02
CUI: C0236788
Disease: Bipolar II disorder
Bipolar II disorder
0 12 0 0 1 1.5E-02
CUI: C0236792
Disease: Asperger Syndrome
Asperger Syndrome
0 3 0 0 1 1.7E-02
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction
0 1 0 0 1 1.8E-02
CUI: C0242129
Disease: Thrombotic stroke
Thrombotic stroke
0 1 0 0 1 1.8E-02
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency
0 14 0 0 1 1.4E-02
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2
0 1 0 0 1 1.8E-02
5,10-Methylenetetrahydrofolate reductase deficiency
0 6 0 0 1 1.6E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis
0 1 0 0 1 1.8E-02
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency
0 52 0 0 1 9.3E-03
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
Stage IV Prostate Carcinoma
0 6 0 0 1 1.6E-02
Non-arteritic ischemic optic neuropathy
0 3 0 0 1 1.7E-02
CUI: C0338573
Disease: Cerebral venous sinus thrombosis
Cerebral venous sinus thrombosis
0 1 0 0 1 1.8E-02
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction
0 1 0 0 1 1.8E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 1.8E-02
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia
0 1 0 0 1 1.8E-02
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia
0 3 0 0 1 1.7E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 1.8E-02