Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
(Idiopathic) normal pressure hydrocephalus
14 0 1 2.8E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.3E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 2.7E-02 0 0
5,10-Methylenetetrahydrofolate reductase deficiency
6 0 1 3.6E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 2.2E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 2 6.2E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.1E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 3 3.2E-03 0 0
Abnormal cardiac exercise stress test
16 0 7 0.22 0 0
CUI: C4021038
Disease: Abnormal circulating renin
Abnormal circulating renin
5 0 1 3.7E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 1 1.2E-02 0 0
Abnormal form of the vertebral bodies
89 0 1 9.0E-03 0 0
CUI: C0278061
Disease: Abnormal mental state
Abnormal mental state
24 0 1 2.2E-02 0 0
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function
21 0 1 2.3E-02 0 0
CUI: C0855742
Disease: Abnormal platelet morphology
Abnormal platelet morphology
10 0 1 3.1E-02 0 0
CUI: C4022866
Disease: Abnormal platelet shape
Abnormal platelet shape
1 0 1 4.3E-02 0 0
CUI: C4022448
Disease: Abnormal prolactin level
Abnormal prolactin level
9 0 1 3.2E-02 0 0
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave
20 0 7 0.19 0 0
CUI: C4025731
Disease: Abnormal thrombosis
Abnormal thrombosis
13 0 1 2.9E-02 0 0
Abnormality of circulating adrenocorticotropin level
6 0 1 3.6E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel
96 0 1 8.5E-03 0 0
Abnormality of female external genitalia
15 0 1 2.7E-02 0 0
Abnormality of immune system physiology
42 0 1 1.6E-02 0 0
CUI: C4025650
Disease: Abnormality of lipid metabolism
Abnormality of lipid metabolism
1 0 1 4.3E-02 0 0
CUI: C4073214
Disease: Abnormality of masseter muscle
Abnormality of masseter muscle
2 0 1 4.2E-02 0 0