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: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 1 1.4E-02 0 0
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency
1 0 1 1.6E-02 0 0
17-Alpha-Hydroxylase/17,20 Lyase Deficiency
4 0 1 1.5E-02 0 0
2-oxo-hept-3-ene-1,7-dioate hydratase activity
14 0 1 1.3E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 3 2.6E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 1.3E-02 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 1.4E-02 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
20 0 1 1.2E-02 0 0
3-METHYLGLUTACONIC ACIDURIA, TYPE VIII
1 0 1 1.6E-02 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 1.1E-02 0 0
6-pyruvoyl-tetrahydropterin synthase deficiency
5 0 1 1.5E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 9.6E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 6.1E-03 0 0
Abdominal obesity metabolic syndrome
10 0 1 1.4E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 6 1.7E-02 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci
7 0 2 2.9E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 7.9E-03 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 2 2.0E-02 0 0
Abnormal atrioventricular conduction
7 0 1 1.4E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 19 2.0E-02 0 0
CUI: C0159060
Disease: Abnormal bowel sounds
Abnormal bowel sounds
5 0 1 1.5E-02 0 0
Abnormal cardiac exercise stress test
16 0 4 5.3E-02 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 1.5E-02 0 0
CUI: C4021038
Disease: Abnormal circulating renin
Abnormal circulating renin
5 0 1 1.5E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 1 8.3E-03 0 0