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: C0276623
Disease: Chronic viral hepatitis
Chronic viral hepatitis
59 0 17 0.13 0 0
CUI: C0022354
Disease: Jaundice, Obstructive
Jaundice, Obstructive
66 0 17 0.12 0 0
Hypocalciuric hypercalcemia, familial, type 1
46 0 14 0.12 0 0
CUI: C0014868
Disease: Esophagitis
Esophagitis
105 0 20 0.12 0 0
CUI: C0041948
Disease: Uremia
Uremia
110 0 19 0.11 0 0
CUI: C0151846
Disease: Periosteal Disorder
Periosteal Disorder
80 0 16 0.11 0 0
CUI: C0008373
Disease: Cholesteatoma
Cholesteatoma
135 0 21 0.10 0 0
CUI: C0574143
Disease: Liver calculus
Liver calculus
45 0 12 1.0E-01 0 0
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency
13 0 9 9.9E-02 0 0
CUI: C0520739
Disease: Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis
47 0 12 9.8E-02 0 0
CUI: C0080032
Disease: Pleural Effusion, Malignant
Pleural Effusion, Malignant
119 0 18 9.6E-02 0 0
CUI: C0267941
Disease: Pancreatitis, Acute Necrotizing
Pancreatitis, Acute Necrotizing
62 0 13 9.6E-02 0 0
CUI: C2936258
Disease: Peri-Implantitis
Peri-Implantitis
62 0 13 9.6E-02 0 0
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis
132 0 19 9.5E-02 0 0
CUI: C0031030
Disease: Periapical Periodontitis
Periapical Periodontitis
90 0 15 9.3E-02 0 0
CUI: C0023531
Disease: Leukoplakia
Leukoplakia
102 0 16 9.2E-02 0 0
CUI: C2931038
Disease: Pancreatic carcinoma, familial
Pancreatic carcinoma, familial
43 0 11 9.2E-02 0 0
CUI: C3639956
Disease: Functional intestinal obstruction
Functional intestinal obstruction
8 0 8 9.2E-02 0 0
CUI: C0267756
Disease: Abscess of peritoneum
Abscess of peritoneum
9 0 8 9.1E-02 0 0
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
9 0 8 9.1E-02 0 0
SUBCORTICAL BAND HETEROTOPIA, X-LINKED
10 0 8 9.0E-02 0 0
CUI: C4021028
Disease: Pseudo-fractures
Pseudo-fractures
10 0 8 9.0E-02 0 0
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia
157 0 20 8.9E-02 0 0
Arteriovenous Malformations, Cerebral
35 0 10 8.9E-02 0 0
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
SPHEROCYTOSIS, TYPE 1 (disorder)
48 0 11 8.9E-02 0 0