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: C4721411
Disease: Osteolysis
Osteolysis
62 0 16 0.13 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 17 0.12 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0
108 0 20 0.12 0 0
CUI: C2937365
Disease: Recurrent aphthous ulcer
Recurrent aphthous ulcer
80 0 17 0.12 0 0
CUI: C0022575
Disease: Keratoconjunctivitis Sicca
Keratoconjunctivitis Sicca
90 0 18 0.12 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 20 0.12 0 0
CUI: C0027543
Disease: Avascular necrosis of bone
Avascular necrosis of bone
73 0 16 0.12 0 0
CUI: C0018920
Disease: Hemangioma, Cavernous
Hemangioma, Cavernous
36 0 12 0.12 0 0
CUI: C0009676
Disease: Confusion
Confusion
75 0 16 0.12 0 0
CUI: C4021977
Disease: Visceral angiomatosis
Visceral angiomatosis
17 0 10 0.11 0 0
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
117 0 20 0.11 0 0
CUI: C0917798
Disease: Cerebral Ischemia
Cerebral Ischemia
120 0 20 0.11 0 0
CUI: C0030554
Disease: Paresthesia
Paresthesia
121 0 20 0.11 0 0
CUI: C1861975
Disease: Cafe au lait spots, multiple
Cafe au lait spots, multiple
61 0 14 0.11 0 0
CUI: C0032231
Disease: Pleurisy
Pleurisy
82 0 16 0.11 0 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
93 0 17 0.11 0 0
CUI: C1298180
Disease: Single tumor
Single tumor
63 0 14 0.11 0 0
CUI: C0026266
Disease: Mitral Valve Insufficiency
Mitral Valve Insufficiency
94 0 17 0.11 0 0
CUI: C3272802
Disease: Hamartomatous polyposis
Hamartomatous polyposis
23 0 10 0.11 0 0
CUI: C1969913
Disease: Generalized hyperkeratosis
Generalized hyperkeratosis
16 0 9 0.10 0 0
CUI: C4022020
Disease: Mucosal telangiectasiae
Mucosal telangiectasiae
16 0 9 0.10 0 0
CUI: C0162834
Disease: Hyperpigmentation
Hyperpigmentation
73 0 14 0.10 0 0
CUI: C0003862
Disease: Arthralgia
Arthralgia
248 0 30 0.10 0 0
CUI: C0042571
Disease: Vertigo
Vertigo
173 0 23 1.0E-01 0 0
CUI: C4025896
Disease: Abnormality of the penis
Abnormality of the penis
8 0 8 1.0E-01 0 0