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: C1840061
Disease: SMALL PATELLA SYNDROME
SMALL PATELLA SYNDROME 		21 15 20 0.57 9 0.60
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 7 0.14 1 7.7E-02
CUI: C1868251
Disease: Neonatal alloimmune thrombocytopenia (NAIT)
Neonatal alloimmune thrombocytopenia (NAIT) 		6 0 4 0.11 0 0
CUI: C2609046
Disease: Sticky platelet syndrome
Sticky platelet syndrome 		6 2 4 0.11 2 0.22
CUI: C1696701
Disease: Skin-picking
Skin-picking 		10 0 4 1.0E-01 0 0
CUI: C0031572
Disease: Phobia, Social
Phobia, Social 		33 0 6 9.8E-02 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 3 4 9.8E-02 1 9.1E-02
CUI: C0234166
Disease: Hyperexplexia
Hyperexplexia 		13 0 4 9.3E-02 0 0
CUI: C2586031
Disease: Hereditary antithrombin III deficiency
Hereditary antithrombin III deficiency 		3 0 3 8.8E-02 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		19 14 4 8.2E-02 1 4.5E-02
CUI: C0743332
Disease: Focal Dystonia
Focal Dystonia 		21 0 4 7.8E-02 0 0
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		35 0 5 7.8E-02 0 0
CUI: C3826457
Disease: Diabetes in children
Diabetes in children 		22 0 4 7.7E-02 0 0
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 8 7.1E-02 2 3.8E-02
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 5 7.1E-02 2 5.4E-02
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 52 4 7.0E-02 1 1.7E-02
CUI: C0338430
Disease: Limbic Encephalitis
Limbic Encephalitis 		27 0 4 7.0E-02 0 0
CUI: C0270500
Disease: Coprophilia (disorder)
Coprophilia (disorder) 		12 0 3 7.0E-02 0 0
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		44 0 5 6.8E-02 0 0
CUI: C0857177
Disease: Arthritic pain
Arthritic pain 		13 0 3 6.8E-02 0 0
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 0 4 6.8E-02 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 3 6.7E-02 0 0
CUI: C0029134
Disease: Optic Neuritis
Optic Neuritis 		79 0 7 6.6E-02 0 0
CUI: C0221028
Disease: Neonatal thrombocytopenia (disorder)
Neonatal thrombocytopenia (disorder) 		15 0 3 6.5E-02 0 0
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		48 61 5 6.5E-02 1 1.4E-02