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: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
93 0 39 0.22 0 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment
84 0 33 0.19 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality
23 0 22 0.18 0 0
CUI: C0032231
Disease: Pleurisy
Pleurisy
82 0 31 0.18 0 0
CUI: C0019079
Disease: Hemoptysis
Hemoptysis
67 0 28 0.18 0 0
CUI: C0030554
Disease: Paresthesia
Paresthesia
121 0 36 0.18 0 0
CUI: C0017086
Disease: Gangrene
Gangrene
69 0 28 0.17 0 0
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax
49 0 25 0.17 0 0
CUI: C0031046
Disease: Pericarditis
Pericarditis
51 0 25 0.17 0 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction
87 0 30 0.17 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood
46 0 24 0.17 0 0
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
117 0 34 0.17 0 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
91 0 30 0.17 0 0
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting
257 0 53 0.16 0 0
CUI: C0151942
Disease: Arterial thrombosis
Arterial thrombosis
33 0 21 0.16 0 0
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
358 0 65 0.16 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0
108 0 31 0.16 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
175 0 40 0.16 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption
175 0 40 0.16 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 31 0.16 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 18 57 0.16 1 5.3E-02
CUI: C0231528
Disease: Myalgia
Myalgia
226 0 46 0.15 0 0
CUI: C0003123
Disease: Anorexia
Anorexia
242 0 46 0.15 0 0
CUI: C0040147
Disease: Thyroiditis
Thyroiditis
104 0 28 0.14 0 0
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome
239 0 44 0.14 0 0