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: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment
84 0 42 0.16 0 0
CUI: C0917798
Disease: Cerebral Ischemia
Cerebral Ischemia
120 0 46 0.15 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 18 69 0.15 1 2.6E-02
Creatine phosphokinase serum increased
228 43 57 0.14 2 3.2E-02
CUI: C0003862
Disease: Arthralgia
Arthralgia
248 27 59 0.14 6 0.14
CUI: C0030554
Disease: Paresthesia
Paresthesia
121 0 42 0.14 0 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
536 87 88 0.13 3 2.8E-02
CUI: C0268731
Disease: Renal glomerular disease
Renal glomerular disease
221 0 50 0.13 0 0
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting
257 0 54 0.13 0 0
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
512 0 80 0.12 0 0
CUI: C0015672
Disease: Fatigue
Fatigue
760 67 106 0.12 1 1.1E-02
CUI: C0027121
Disease: Myositis
Myositis
254 0 51 0.12 0 0
CUI: C0026848
Disease: Myopathy
Myopathy
634 166 91 0.12 3 1.6E-02
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 35 0.11 0 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
93 0 32 0.11 0 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction
87 0 31 0.11 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0
108 0 33 0.11 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 33 0.11 0 0
CUI: C0003123
Disease: Anorexia
Anorexia
242 0 46 0.11 0 0
CUI: C0037763
Disease: Spasm
Spasm
172 9 39 0.11 1 3.3E-02
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
91 0 31 0.11 0 0
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage
122 0 34 0.11 0 0
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
279 0 49 0.11 0 0
CUI: C0332563
Disease: Papule
Papule
76 0 29 0.11 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 34 0.11 0 0