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 2 6.5E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 2 2.8E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 3 4.9E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 1 1.8E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 1.7E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 2 1.7E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 2 6.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 3 9.4E-03 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 3.7E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 7 7.6E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 1.1E-02 0 0
Abnormal form of the vertebral bodies
89 0 1 9.3E-03 0 0
CUI: C4025715
Disease: Abnormal large intestine morphology
Abnormal large intestine morphology
2 0 1 5.0E-02 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation
32 0 1 2.0E-02 0 0
CUI: C0278061
Disease: Abnormal mental state
Abnormal mental state
24 0 3 7.5E-02 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 1 3.0E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 1 1.3E-02 0 0
CUI: C0855742
Disease: Abnormal platelet morphology
Abnormal platelet morphology
10 0 1 3.6E-02 0 0
Abnormal serum dehydroepiandrosterone level
1 0 1 5.3E-02 0 0
Abnormal subcutaneous fat tissue distribution
9 0 1 3.7E-02 0 0
Abnormality of cardiovascular system morphology
198 0 1 4.6E-03 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel
96 0 1 8.8E-03 0 0
Abnormality of metabolism/homeostasis
171 0 2 1.1E-02 0 0
Abnormality of reproductive system physiology
1 0 1 5.3E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.3E-03 0 0