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: C4021234
Disease: 2-4 toe syndactyly
2-4 toe syndactyly
2 0 1 5.3E-02 0 0
3-methylcrotonyl CoA carboxylase 1 deficiency
5 0 2 9.5E-02 0 0
3-methylcrotonyl CoA carboxylase 2 deficiency
1 0 1 5.6E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 8.3E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 3.3E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.1E-03 0 0
Abnormal atrioventricular conduction
7 0 1 4.2E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 3 3.2E-03 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 4.8E-02 0 0
Abnormal electrophysiology of sinoatrial node origin
1 0 1 5.6E-02 0 0
CUI: C4021662
Disease: Abnormal endocardium morphology
Abnormal endocardium morphology
23 0 2 5.1E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 2.2E-02 0 0
Abnormal form of the vertebral bodies
89 0 1 9.4E-03 0 0
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl
5 0 2 9.5E-02 0 0
CUI: C4531142
Disease: Abnormal lymphocyte physiology
Abnormal lymphocyte physiology
1 0 1 5.6E-02 0 0
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology
40 0 1 1.8E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 2 2.7E-02 0 0
CUI: C0151854
Disease: Abnormal platelets
Abnormal platelets
11 0 2 7.4E-02 0 0
CUI: C4025731
Disease: Abnormal thrombosis
Abnormal thrombosis
13 0 1 3.3E-02 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology
6 0 2 9.1E-02 0 0
CUI: C0241665
Disease: Abnormal venous morphology
Abnormal venous morphology
2 0 1 5.3E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 7.6E-03 0 0
CUI: C4025845
Disease: Abnormality iris morphology
Abnormality iris morphology
27 0 1 2.3E-02 0 0
Abnormality of circulating leptin level
1 0 1 5.6E-02 0 0
CUI: C4025213
Disease: Abnormality of complement system
Abnormality of complement system
2 0 1 5.3E-02 0 0