Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
46, XX Testicular Disorders of Sex Development
11 0 1 3.7E-02 0 0
CUI: C4479552
Disease: 46,XX SEX REVERSAL 4
46,XX SEX REVERSAL 4
3 0 1 5.3E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 1.7E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 4 3.4E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 2.6E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 5 1.6E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 3.0E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 2 2.5E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 2.8E-02 0 0
CUI: C4022863
Disease: Abnormal alpha granule content
Abnormal alpha granule content
1 0 1 5.9E-02 0 0
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology
3 0 1 5.3E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 4 4.3E-03 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 1 1.9E-02 0 0
CUI: C4021839
Disease: Abnormal dense granule content
Abnormal dense granule content
1 0 1 5.9E-02 0 0
CUI: C4022924
Disease: Abnormal eye physiology
Abnormal eye physiology
6 0 1 4.5E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 2.2E-02 0 0
Abnormal internal carotid artery morphology
7 0 1 4.3E-02 0 0
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement
22 0 1 2.6E-02 0 0
CUI: C1834387
Disease: Abnormal iris pigmentation
Abnormal iris pigmentation
2 0 1 5.6E-02 0 0
CUI: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology
30 0 2 4.4E-02 0 0
Abnormal mitochondria in muscle tissue
39 0 1 1.8E-02 0 0
CUI: C1291045
Disease: Abnormal peristalsis
Abnormal peristalsis
1 0 1 5.9E-02 0 0
CUI: C4025250
Disease: Abnormal sacrum morphology
Abnormal sacrum morphology
17 0 1 3.0E-02 0 0
CUI: C4531122
Disease: Abnormal speech prosody
Abnormal speech prosody
15 0 1 3.2E-02 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 1 1.4E-02 0 0