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: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne
360 6 60 0.13 1 0.11
CUI: C0282193
Disease: Iron Overload
Iron Overload
235 0 45 0.13 0 0
CUI: C0031030
Disease: Periapical Periodontitis
Periapical Periodontitis
85 0 28 0.13 0 0
CUI: C0276138
Disease: Viral myocarditis
Viral myocarditis
128 0 32 0.12 0 0
CUI: C0856742
Disease: Post MI
Post MI
203 0 39 0.12 0 0
CUI: C3714948
Disease: PACHYONYCHIA CONGENITA 3
PACHYONYCHIA CONGENITA 3
208 0 39 0.12 0 0
CUI: C0342649
Disease: Vascular calcification
Vascular calcification
255 0 43 0.11 0 0
CUI: C0027121
Disease: Myositis
Myositis
187 3 36 0.11 1 0.17
TNF receptor-associated periodic fever syndrome (TRAPS)
90 0 26 0.11 0 0
CUI: C0432283
Disease: Osteoglophonic dwarfism
Osteoglophonic dwarfism
100 0 27 0.11 0 0
CUI: C0234233
Disease: Sore to touch
Sore to touch
56 8 22 0.11 1 9.1E-02
CUI: C0036472
Disease: Scrub Typhus
Scrub Typhus
58 0 22 0.11 0 0
CUI: C0038525
Disease: Subarachnoid Hemorrhage
Subarachnoid Hemorrhage
452 0 61 0.11 0 0
CUI: C0030552
Disease: Paresis
Paresis
213 0 37 0.11 0 0
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy
83 0 24 0.11 0 0
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis
272 0 42 0.11 0 0
CUI: C0231528
Disease: Myalgia
Myalgia
107 0 26 0.11 0 0
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
211 0 36 0.11 0 0
CUI: C0949664
Disease: Tauopathies
Tauopathies
243 0 39 0.11 0 0
CUI: C0019202
Disease: Hepatolenticular Degeneration
Hepatolenticular Degeneration
129 0 28 0.11 0 0
CUI: C0027059
Disease: Myocarditis
Myocarditis
266 0 41 0.11 0 0
CUI: C0041948
Disease: Uremia
Uremia
89 0 24 0.11 0 0
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency
89 0 24 0.11 0 0
CUI: C0011633
Disease: Dermatomyositis
Dermatomyositis
227 0 37 0.10 0 0
Respiratory Distress Syndrome, Newborn
143 0 29 0.10 0 0