Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
(Idiopathic) normal pressure hydrocephalus
14 0 1 1.0E-02 0 0
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 1 1.1E-02 0 0
CUI: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
20 0 1 9.8E-03 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 1 1.1E-02 0 0
17-Hydroxysteroid Dehydrogenase Deficiency
5 0 1 1.1E-02 0 0
2,4-Dienoyl-CoA Reductase Deficiency
2 0 1 1.2E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 6.0E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 7.3E-03 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 1 8.8E-03 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 1 1.1E-02 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 1.1E-02 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
20 0 1 9.8E-03 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 3 2.7E-02 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome
4 0 1 1.2E-02 0 0
6-Phosphogluconolactonase Deficiency
1 0 1 1.2E-02 0 0
6-pyruvoyl-tetrahydropterin synthase deficiency
5 0 4 4.8E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 3 2.5E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 2 1.6E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 2 1.1E-02 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 1.1E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 2 1.9E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 7 1.9E-02 0 0
CUI: C3826804
Disease: Abdominal pain in children
Abdominal pain in children
2 0 1 1.2E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 1 1.0E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 1.0E-02 0 0