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 1 2.3E-02 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 1 2.1E-02 0 0
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency
1 0 1 2.6E-02 0 0
17-Alpha-Hydroxylase/17,20 Lyase Deficiency
4 0 1 2.4E-02 0 0
CUI: C4021234
Disease: 2-4 toe syndactyly
2-4 toe syndactyly
2 0 1 2.5E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.1E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 9 0.15 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 9 0.21 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 2.1E-02 0 0
3-methylcrotonyl CoA carboxylase 1 deficiency
5 0 1 2.3E-02 0 0
3-methylcrotonyl CoA carboxylase 2 deficiency
1 0 1 2.6E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 1 1.5E-02 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome
4 0 1 2.4E-02 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 1.5E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 1.6E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 3 4.1E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 1.3E-02 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess
4 0 1 2.4E-02 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 2 4.3E-02 0 0
CUI: C1142110
Disease: Abdominal Compartment Syndrome
Abdominal Compartment Syndrome
2 0 1 2.5E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 2.0E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 2 5.9E-03 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 1.8E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 1.7E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 3 3.9E-02 0 0