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: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
7 0 1 7.2E-03 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 2 9.3E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 5.3E-03 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 6.8E-03 0 0
CUI: C4023115
Disease: 3-4 finger cutaneous syndactyly
3-4 finger cutaneous syndactyly
3 0 1 7.4E-03 0 0
3-@METHYLGLUTACONIC ACIDURIA, TYPE V
3 0 1 7.4E-03 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
20 0 1 6.6E-03 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 2 1.2E-02 0 0
CUI: C4039473
Disease: 3-methylglutaconic aciduria type 5
3-methylglutaconic aciduria type 5
1 0 1 7.5E-03 0 0
CUI: C3151952
Disease: 3-Methylglutaric aciduria
3-Methylglutaric aciduria
3 0 1 7.4E-03 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 6.2E-03 0 0
CUI: C4510744
Disease: 46,XY partial gonadal dysgenesis
46,XY partial gonadal dysgenesis
11 0 1 7.0E-03 0 0
CUI: C4015129
Disease: 46,XY SEX REVERSAL 9
46,XY SEX REVERSAL 9
2 0 1 7.5E-03 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 1 5.9E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 2 8.5E-03 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 6.5E-03 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
9 0 1 7.1E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 32 7.9E-02 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 7.1E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 3 1.5E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 6.6E-03 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 5.8E-03 0 0
CUI: C4703464
Disease: Abnormal aortic valve physiology
Abnormal aortic valve physiology
4 0 3 2.2E-02 0 0
Abnormal atrioventricular conduction
7 0 1 7.2E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 23 2.3E-02 0 0