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 5.0E-02 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 1 4.2E-02 0 0
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency
1 0 1 6.7E-02 0 0
17-Alpha-Hydroxylase/17,20 Lyase Deficiency
4 0 1 5.6E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.4E-02 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 4.3E-02 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 2.3E-02 0 0
6-pyruvoyl-tetrahydropterin synthase deficiency
5 0 2 0.11 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 1.8E-02 0 0
CUI: C0232487
Disease: Abdominal discomfort
Abdominal discomfort
3 0 1 5.9E-02 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
9 0 1 4.3E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 2 6.3E-03 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci
7 0 1 4.8E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.3E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 1.8E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 9 9.8E-03 0 0
CUI: C4021982
Disease: Abnormal eating behavior
Abnormal eating behavior
8 0 1 4.5E-02 0 0
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement
22 0 2 5.7E-02 0 0
CUI: C4551596
Disease: Abnormal renal morphology
Abnormal renal morphology
35 0 1 2.0E-02 0 0
CUI: C4021821
Disease: Abnormality of the urinary system
Abnormality of the urinary system
50 0 1 1.6E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 3.8E-02 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation
111 0 1 8.0E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 0 7 3.3E-02 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
64 0 1 1.3E-02 0 0
CUI: C1321756
Disease: Achalasia
Achalasia
40 0 2 3.8E-02 0 0