Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Colorectal Signet Ring Cell Carcinoma
8 0 3 0.21 0 0
CUI: C1740836
Disease: Acute migraine
Acute migraine
8 0 3 0.21 0 0
CUI: C0028432
Disease: Nose Diseases
Nose Diseases
14 0 4 0.21 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis
9 0 3 0.20 0 0
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion
9 0 3 0.20 0 0
CUI: C0269155
Disease: Germinal inclusion cyst of ovary
Germinal inclusion cyst of ovary
3 0 2 0.20 0 0
CUI: C1868081
Disease: Juvenile Polyposis Coli
Juvenile Polyposis Coli
9 0 3 0.20 0 0
Isovaleryl-CoA dehydrogenase deficiency
22 0 5 0.19 0 0
CUI: C0267055
Disease: Erosive esophagitis
Erosive esophagitis
16 0 4 0.19 0 0
CUI: C0029441
Disease: Osteoid osteoma
Osteoid osteoma
10 0 3 0.19 0 0
CUI: C0581384
Disease: Chronic anemia
Chronic anemia
10 0 3 0.19 0 0
CUI: C0747742
Disease: polyp benign
polyp benign
10 0 3 0.19 0 0
CUI: C3495831
Disease: Aluminium overload
Aluminium overload
10 0 3 0.19 0 0
CUI: C1168250
Disease: Laryngopharyngeal Reflux
Laryngopharyngeal Reflux
23 0 5 0.19 0 0
CUI: C0154051
Disease: Hemangioma of retina
Hemangioma of retina
4 0 2 0.18 0 0
Remitting seronegative symmetrical synovitis with pitting oedema syndrome
4 0 2 0.18 0 0
CUI: C0007361
Disease: Cat-Scratch Disease
Cat-Scratch Disease
11 0 3 0.18 0 0
CUI: C0221725
Disease: Bronchial Obstruction
Bronchial Obstruction
11 0 3 0.18 0 0
Congenital Nephrogenic Diabetes Insipidus
11 0 3 0.18 0 0
CUI: C0085692
Disease: Hemorrhagic cystitis
Hemorrhagic cystitis
18 0 4 0.17 0 0
CUI: C0010673
Disease: Endometrial cystic hyperplasia
Endometrial cystic hyperplasia
5 0 2 0.17 0 0
CUI: C1960443
Disease: Vasculitic neuropathy
Vasculitic neuropathy
13 0 3 0.16 0 0
CUI: C2721566
Disease: Meniscal degeneration
Meniscal degeneration
13 0 3 0.16 0 0
CUI: C0034215
Disease: Pyometra
Pyometra
6 0 2 0.15 0 0
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder
29 0 5 0.15 0 0