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 3.6E-03 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 1 3.6E-03 0 0
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
7 0 1 3.7E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 3 9.5E-03 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 3 1.0E-02 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 3 1.1E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 3.6E-03 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3
12 0 1 3.6E-03 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 3.4E-03 0 0
CUI: C4510744
Disease: 46,XY partial gonadal dysgenesis
46,XY partial gonadal dysgenesis
11 0 1 3.6E-03 0 0
CUI: C4015129
Disease: 46,XY SEX REVERSAL 9
46,XY SEX REVERSAL 9
2 0 2 7.5E-03 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 4 1.3E-02 0 0
CUI: C4304529
Disease: 5q14.3 microdeletion syndrome
5q14.3 microdeletion syndrome
1 0 1 3.8E-03 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 2 6.6E-03 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 2 6.6E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 3 8.2E-03 0 0
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism
8 0 2 7.4E-03 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 3.5E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 3.6E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 18 13 2.3E-02 1 2.1E-03
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 3.6E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 3 9.2E-03 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 3.5E-03 0 0
CUI: C4022863
Disease: Abnormal alpha granule content
Abnormal alpha granule content
1 0 1 3.8E-03 0 0
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology
3 0 1 3.7E-03 0 0