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 1.0E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 9 6.5E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 10 8.8E-02 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 10 0.11 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 2 1.7E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3
12 0 1 9.7E-03 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome
4 0 1 1.1E-02 0 0
46, XX Testicular Disorders of Sex Development
11 0 2 2.0E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 8.6E-03 0 0
CUI: C3151782
Disease: 46,XX SEX REVERSAL 3
46,XX SEX REVERSAL 3
1 0 1 1.1E-02 0 0
CUI: C4479552
Disease: 46,XX SEX REVERSAL 4
46,XX SEX REVERSAL 4
3 0 1 1.1E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome
1 0 1 1.1E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 5.2E-03 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 3 2.7E-02 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
9 0 1 1.0E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 20 5.3E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 9.3E-03 0 0
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect
8 0 1 1.0E-02 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 1.0E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 2 1.3E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 9.0E-03 0 0
CUI: C4021524
Disease: Abnormal adipose tissue morphology
Abnormal adipose tissue morphology
6 0 1 1.0E-02 0 0
CUI: C0266781
Disease: Abnormal amniotic fluid
Abnormal amniotic fluid
8 0 2 2.0E-02 0 0
CUI: C4703464
Disease: Abnormal aortic valve physiology
Abnormal aortic valve physiology
4 0 3 3.2E-02 0 0
CUI: C4021748
Disease: Abnormal B cell morphology
Abnormal B cell morphology
1 0 1 1.1E-02 0 0