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: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 2 3.0E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome
1 0 1 7.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C4021208
Disease: Abnormal B cell count
Abnormal B cell count
2 0 2 0.15 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 2 2.2E-03 0 0
CUI: C4021803
Disease: Abnormal eyelid morphology
Abnormal eyelid morphology
10 0 3 0.15 0 0
CUI: C1855755
Disease: Abnormal immunoglobulin level
Abnormal immunoglobulin level
6 0 3 0.19 0 0
CUI: C4021036
Disease: Abnormal natural killer cell count
Abnormal natural killer cell count
3 0 2 0.14 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology
12 0 1 4.2E-02 0 0
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology
40 0 1 1.9E-02 0 0
CUI: C4025810
Disease: Abnormal palmar dermatoglyphics
Abnormal palmar dermatoglyphics
5 0 1 5.9E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 1 1.4E-02 0 0
CUI: C4021984
Disease: Abnormal soft palate morphology
Abnormal soft palate morphology
3 0 1 6.7E-02 0 0
CUI: C4021113
Disease: Abnormal T cell count
Abnormal T cell count
2 0 2 0.15 0 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve
50 0 1 1.6E-02 0 0
Abnormality of blood and blood-forming tissues
23 0 1 2.9E-02 0 0
CUI: C4025901
Disease: Abnormality of body height
Abnormality of body height
18 0 1 3.3E-02 0 0
Abnormality of bone marrow cell morphology
15 0 3 0.12 0 0
CUI: C4021657
Disease: Abnormality of bone mineral density
Abnormality of bone mineral density
22 0 1 2.9E-02 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 1 8.6E-03 0 0
Abnormality of cardiovascular system morphology
198 0 2 9.6E-03 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability
34 0 2 4.4E-02 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology
86 0 1 1.0E-02 0 0
Abnormality of female external genitalia
15 0 1 3.7E-02 0 0
Abnormality of female internal genitalia
31 0 1 2.3E-02 0 0