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: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 9.2E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.3E-02 0 0
CUI: C3669122
Disease: 5-Alpha Reductase Deficiency
5-Alpha Reductase Deficiency
8 0 1 3.1E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 1.5E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 8 6.7E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 2.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.1E-03 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 2.4E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 3 3.2E-03 0 0
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 1 2.8E-02 0 0
CUI: C4025630
Disease: Abnormal bone structure
Abnormal bone structure
7 0 1 3.2E-02 0 0
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement
7 0 1 3.2E-02 0 0
CUI: C4022657
Disease: Abnormal drinking behavior
Abnormal drinking behavior
1 0 1 4.0E-02 0 0
CUI: C4021982
Disease: Abnormal eating behavior
Abnormal eating behavior
8 0 1 3.1E-02 0 0
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology
40 0 1 1.6E-02 0 0
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function
21 0 1 2.2E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel
96 0 1 8.3E-03 0 0
Abnormality of metabolism/homeostasis
171 0 2 1.0E-02 0 0
CUI: C4025871
Disease: Abnormality of the face
Abnormality of the face
31 0 1 1.8E-02 0 0
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system
34 0 1 1.7E-02 0 0
CUI: C4021745
Disease: Abnormality of the musculature
Abnormality of the musculature
24 0 1 2.1E-02 0 0
Abnormality of the parathyroid gland
2 0 1 3.8E-02 0 0
Abnormality of the parathyroid physiology
1 0 1 4.0E-02 0 0
CUI: C4021754
Disease: Abnormality of the sella turcica
Abnormality of the sella turcica
3 0 1 3.7E-02 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
148 0 4 2.4E-02 0 0