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: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 2 1.9E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 6.3E-03 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 1 7.5E-03 0 0
CUI: C2936403
Disease: 46, XX Disorders of Sex Development
46, XX Disorders of Sex Development
6 0 1 9.2E-03 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 7.8E-03 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 7 5.2E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 2 9.8E-03 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess
4 0 1 9.3E-03 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 2 1.8E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 7.9E-03 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
9 0 1 8.9E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 11 2.8E-02 0 0
CUI: C3826804
Disease: Abdominal pain in children
Abdominal pain in children
2 0 1 9.5E-03 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 8.3E-03 0 0
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness
2 0 1 9.5E-03 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 9.5E-03 0 0
CUI: C0919934
Disease: Abdominal wall infection
Abdominal wall infection
1 0 1 9.6E-03 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci
7 0 2 1.8E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 3 2.1E-02 0 0
Abnormal axonemal organization of respiratory motile cilia
3 0 2 1.9E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 23 2.3E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 5.6E-03 0 0
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 1 8.7E-03 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology
32 0 2 1.5E-02 0 0
Abnormal central microtubular pair morphology of respiratory motile cilia
2 0 2 1.9E-02 0 0