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: C0025281
Disease: Meniere Disease
Meniere Disease
69 36 17 0.14 14 0.23
Gastro-esophageal reflux disease with esophagitis
71 0 17 0.13 0 0
Aggressive periodontitis, generalized
56 16 15 0.13 1 1.9E-02
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis
53 0 14 0.13 0 0
CUI: C0031736
Disease: Polymorphous light eruption
Polymorphous light eruption
20 0 10 0.12 0 0
CUI: C0151450
Disease: Secondary Sjögren's syndrome
Secondary Sjögren's syndrome
20 0 10 0.12 0 0
CUI: C0014869
Disease: Peptic Esophagitis
Peptic Esophagitis
85 0 17 0.12 0 0
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion
76 15 16 0.12 7 0.15
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome
77 10 16 0.12 2 4.3E-02
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases
69 0 15 0.12 0 0
Idiopathic Membranous Glomerulonephritis
79 13 16 0.12 1 2.0E-02
CUI: C0340170
Disease: Complicated pneumoconiosis
Complicated pneumoconiosis
13 0 9 0.12 0 0
CUI: C0019100
Disease: Severe Dengue
Severe Dengue
117 0 20 0.12 0 0
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
51 72 13 0.12 1 9.2E-03
CUI: C0338437
Disease: Neurocysticercosis
Neurocysticercosis
34 9 11 0.12 1 2.2E-02
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia
64 0 14 0.11 0 0
CUI: C0023891
Disease: Liver Cirrhosis, Alcoholic
Liver Cirrhosis, Alcoholic
126 15 20 0.11 2 3.9E-02
CUI: C0042341
Disease: Varicocele
Varicocele
99 3 17 0.11 1 2.5E-02
CUI: C1563937
Disease: Atherogenesis
Atherogenesis
59 0 13 0.11 0 0
CUI: C3714757
Disease: Juvenile rheumatoid arthritis
Juvenile rheumatoid arthritis
183 0 25 0.11 0 0
CUI: C0013295
Disease: Duodenal Ulcer
Duodenal Ulcer
102 0 17 0.11 0 0
CUI: C0014743
Disease: Erythema Nodosum
Erythema Nodosum
51 0 12 0.11 0 0
CUI: C0032533
Disease: Polymyalgia Rheumatica
Polymyalgia Rheumatica
51 7 12 0.11 1 2.3E-02
CUI: C0262988
Disease: Vasculitis of the skin
Vasculitis of the skin
21 0 9 0.11 0 0
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
Nephrotic Syndrome, Minimal Change
85 10 15 0.11 1 2.1E-02