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: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 2.2E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 9.4E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.3E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 2 2.2E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 1.3E-02 0 0
Abnormal delayed hypersensitivity skin test
1 0 1 0.25 0 0
CUI: C0855999
Disease: Abnormal eosinophil morphology
Abnormal eosinophil morphology
3 0 2 0.40 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 3.1E-02 0 0
CUI: C2675111
Disease: Abnormal eyelash morphology
Abnormal eyelash morphology
39 0 1 2.4E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 1 1.6E-02 0 0
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function
21 0 1 4.2E-02 0 0
CUI: C0855742
Disease: Abnormal platelet morphology
Abnormal platelet morphology
10 0 1 7.7E-02 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 1 9.3E-03 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
59 0 1 1.6E-02 0 0
Abnormality of female internal genitalia
31 0 1 2.9E-02 0 0
CUI: C4025888
Disease: Abnormality of the menstrual cycle
Abnormality of the menstrual cycle
11 0 1 7.1E-02 0 0
CUI: C4021745
Disease: Abnormality of the musculature
Abnormality of the musculature
24 0 1 3.7E-02 0 0
Abnormality of the periventricular white matter
45 0 1 2.1E-02 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx
23 0 1 3.8E-02 0 0
CUI: C1860493
Disease: Abnormality of the sternum
Abnormality of the sternum
46 0 1 2.0E-02 0 0
Absent microvilli on the surface of peripheral blood lymphocytes
1 0 1 0.25 0 0
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 4.3E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 8.1E-03 0 0
Acute exacerbation of chronic obstructive airways disease
63 0 1 1.5E-02 0 0
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
639 0 1 1.6E-03 0 0