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: C0001193
Disease: Apert syndrome
Apert syndrome
1 0 1 5.3E-02 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
13 0 1 3.2E-02 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
9 0 1 3.7E-02 0 0
CUI: C0003467
Disease: Anxiety
Anxiety
13 0 1 3.2E-02 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
15 0 1 3.0E-02 0 0
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
5 0 1 4.3E-02 0 0
CUI: C0005697
Disease: Neurogenic Urinary Bladder
Neurogenic Urinary Bladder
7 0 2 8.3E-02 0 0
CUI: C0006325
Disease: Bruxism
Bruxism
4 0 1 4.5E-02 0 0
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
16 0 1 2.9E-02 0 0
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm
16 0 1 2.9E-02 0 0
CUI: C0008373
Disease: Cholesteatoma
Cholesteatoma
1 0 1 5.3E-02 0 0
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
31 0 2 4.2E-02 0 0
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
Adenoid Cystic Carcinoma
11 0 1 3.4E-02 0 0
CUI: C0011053
Disease: Deafness
Deafness
23 0 1 2.4E-02 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
7 0 1 4.0E-02 0 0
CUI: C0014170
Disease: Endometrial Neoplasms
Endometrial Neoplasms
2 0 1 5.0E-02 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy
32 0 1 2.0E-02 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
30 0 1 2.1E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent
11 0 1 3.4E-02 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma
6 0 1 4.2E-02 0 0
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
22 0 1 2.5E-02 0 0
CUI: C0018671
Disease: Head and Neck Neoplasms
Head and Neck Neoplasms
4 0 1 4.5E-02 0 0
Sensorineural Hearing Loss (disorder)
39 0 1 1.8E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
37 0 2 3.7E-02 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
25 0 1 2.3E-02 0 0