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: C0349622
Disease: Hemangiopericytoma of meninges
Hemangiopericytoma of meninges
2 0 2 0.15 0 0
CUI: C4022033
Disease: Neoplasia of the pleura
Neoplasia of the pleura
2 0 2 0.15 0 0
CUI: C4280764
Disease: Reduced C-peptide level
Reduced C-peptide level
2 0 2 0.15 0 0
CUI: C0347944
Disease: Pelvic mass
Pelvic mass
3 0 2 0.14 0 0
CUI: C4025867
Disease: Abnormality of the forehead
Abnormality of the forehead
4 0 2 0.13 0 0
Jervell And Lange-Nielsen Syndrome 1
4 0 2 0.13 0 0
CUI: C0334511
Disease: Pleural Solitary Fibrous Tumor
Pleural Solitary Fibrous Tumor
5 0 2 0.12 0 0
CUI: C0403654
Disease: Bladder outflow obstruction
Bladder outflow obstruction
5 0 2 0.12 0 0
CUI: C2732413
Disease: Postexertional fatigue
Postexertional fatigue
5 0 2 0.12 0 0
CUI: C0268634
Disease: Disorder of fatty acid metabolism
Disorder of fatty acid metabolism
6 0 2 0.12 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma
8 0 2 0.11 0 0
CUI: C4025698
Disease: Abnormality of the peritoneum
Abnormality of the peritoneum
9 0 2 1.0E-01 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
10 0 2 9.5E-02 0 0
Profound sensorineural hearing impairment
10 0 2 9.5E-02 0 0
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome
11 0 2 9.1E-02 0 0
CUI: C2931173
Disease: Pediatric ulcerative colitis
Pediatric ulcerative colitis
11 0 2 9.1E-02 0 0
CUI: C4022395
Disease: Abnormality of the mediastinum
Abnormality of the mediastinum
12 0 2 8.7E-02 0 0
CUI: C0042258
Disease: Vaginal Neoplasms
Vaginal Neoplasms
13 0 2 8.3E-02 0 0
CUI: C1846288
Disease: Recurrent hypoglycemia
Recurrent hypoglycemia
13 0 2 8.3E-02 0 0
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
13 0 2 8.3E-02 0 0
Medium-chain acyl-coenzyme A dehydrogenase deficiency
15 0 2 7.7E-02 0 0
CUI: C0233612
Disease: Waxy flexibility
Waxy flexibility
15 0 2 7.7E-02 0 0
CUI: C0234447
Disease: Narcosis
Narcosis
1 0 1 7.7E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome
1 0 1 7.7E-02 0 0
Chalasia of lower esophageal sphincter
1 0 1 7.7E-02 0 0