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: C3266731
Disease: 2-methyl-3-hydroxybutyric aciduria
2-methyl-3-hydroxybutyric aciduria
8 0 1 1.6E-02 0 0
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
5 0 1 1.6E-02 0 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
20 0 1 1.3E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 1.2E-02 0 0
6-Phosphogluconolactonase Deficiency
1 0 1 1.8E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 6.3E-03 0 0
CUI: C1142110
Disease: Abdominal Compartment Syndrome
Abdominal Compartment Syndrome
2 0 1 1.7E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 2 2.6E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 6 1.7E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 1 1.4E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 1.4E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 1.7E-02 0 0
CUI: C0919934
Disease: Abdominal wall infection
Abdominal wall infection
1 0 1 1.8E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 1.0E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 7 7.3E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 7.6E-03 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 1 8.7E-03 0 0
CUI: C4021741
Disease: Abnormal cortical bone morphology
Abnormal cortical bone morphology
41 0 2 2.1E-02 0 0
CUI: C0241654
Disease: Abnormal heart valve morphology
Abnormal heart valve morphology
42 0 1 1.0E-02 0 0
CUI: C4021095
Disease: Abnormal hypothalamus morphology
Abnormal hypothalamus morphology
4 0 1 1.7E-02 0 0
CUI: C4025758
Disease: Abnormal myocardium morphology
Abnormal myocardium morphology
19 0 1 1.3E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 5.8E-03 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 1 9.0E-03 0 0
Abnormality of amino acid metabolism
8 0 1 1.6E-02 0 0
Abnormality of blood and blood-forming tissues
23 0 1 1.3E-02 0 0