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: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 18 12 2.5E-02 1 2.0E-02
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 2 1.0E-02 0 0
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness
2 0 1 5.5E-03 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci
7 0 1 5.3E-03 0 0
CUI: C2004632
Disease: aberrant right subclavian artery
aberrant right subclavian artery
2 0 1 5.5E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 4 1.7E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 4.5E-03 0 0
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level
16 0 1 5.1E-03 0 0
CUI: C0266781
Disease: Abnormal amniotic fluid
Abnormal amniotic fluid
8 0 3 1.6E-02 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology
29 0 4 1.9E-02 0 0
CUI: C0522216
Disease: Abnormal auditory evoked potential
Abnormal auditory evoked potential
11 0 2 1.1E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 121 24 2.2E-02 1 6.5E-03
CUI: C4476566
Disease: Abnormal brain choline level by MRS
Abnormal brain choline level by MRS
1 0 1 5.5E-03 0 0
Abnormal brain FDG positron emission tomography
18 0 2 1.0E-02 0 0
CUI: C4476564
Disease: Abnormal brain lactate level by MRS
Abnormal brain lactate level by MRS
2 1 1 5.5E-03 1 2.9E-02
CUI: C1260922
Disease: Abnormal breathing
Abnormal breathing
5 0 1 5.4E-03 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 6 3.2E-02 0 0
Abnormal cardiac ventricle morphology
2 0 1 5.5E-03 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology
32 0 4 1.9E-02 0 0
CUI: C4025711
Disease: Abnormal caudate nucleus morphology
Abnormal caudate nucleus morphology
9 0 1 5.3E-03 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 5.2E-03 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 5.4E-03 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 1 4.6E-03 0 0
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility
9 5 2 1.1E-02 2 5.4E-02
Abnormal circulating follicle-stimulating hormone level
1 0 1 5.5E-03 0 0