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: C0007274
Disease: Carotid Artery Thrombosis
Carotid Artery Thrombosis
30 0 1 3.2E-02 0 0
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders
30 0 1 3.2E-02 0 0
CUI: C3275069
Disease: Chronic Total Occlusion Vessel
Chronic Total Occlusion Vessel
33 0 1 2.9E-02 0 0
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis
35 0 1 2.8E-02 0 0
CUI: C0243010
Disease: Viral Encephalitis
Viral Encephalitis
35 0 1 2.8E-02 0 0
Ostium secundum atrial septal defect
37 0 1 2.6E-02 0 0
CUI: C1264039
Disease: von Willebrand Disease, Type 1
von Willebrand Disease, Type 1
39 0 1 2.5E-02 0 0
CUI: C0013491
Disease: Ecchymosis
Ecchymosis
41 0 1 2.4E-02 0 0
CUI: C0751633
Disease: Carotid Artery Plaque
Carotid Artery Plaque
41 0 1 2.4E-02 0 0
CUI: C0346421
Disease: Chronic eosinophilic leukemia
Chronic eosinophilic leukemia
42 0 1 2.3E-02 0 0
CUI: C1960870
Disease: Transformed migraine
Transformed migraine
43 0 1 2.3E-02 0 0
CUI: C0087086
Disease: Thrombus
Thrombus
46 0 1 2.1E-02 0 0
CUI: C0019080
Disease: Hemorrhage
Hemorrhage
47 0 1 2.1E-02 0 0
ST-segment elevation myocardial infarction (STEMI)
51 0 1 1.9E-02 0 0
CUI: C0242380
Disease: Libman-Sacks Disease
Libman-Sacks Disease
59 0 1 1.7E-02 0 0
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease
62 0 1 1.6E-02 0 0
CUI: C0340076
Disease: Asthmatic pulmonary eosinophilia
Asthmatic pulmonary eosinophilia
62 0 1 1.6E-02 0 0
CUI: C0596240
Disease: Cancer Pain
Cancer Pain
62 0 1 1.6E-02 0 0
CUI: C0020452
Disease: Hyperemia
Hyperemia
64 0 1 1.5E-02 0 0
CUI: C0878773
Disease: Overactive Bladder
Overactive Bladder
65 0 1 1.5E-02 0 0
CUI: C0917996
Disease: Cerebral Aneurysm
Cerebral Aneurysm
65 0 1 1.5E-02 0 0
CUI: C0271160
Disease: Cortical cataract
Cortical cataract
69 0 1 1.4E-02 0 0
CUI: C0034068
Disease: Pulmonary Eosinophilia
Pulmonary Eosinophilia
70 0 1 1.4E-02 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology
70 0 1 1.4E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent
73 0 1 1.4E-02 0 0