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 3.6E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 1.0E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 1 2.3E-02 0 0
CUI: C0232488
Disease: Abdominal colic
Abdominal colic
2 0 1 6.2E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 2 6.3E-03 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 4.3E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 4 4.3E-03 0 0
Abnormal brain FDG positron emission tomography
18 0 1 3.1E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
32 0 1 2.2E-02 0 0
Abnormal form of the vertebral bodies
89 0 2 2.0E-02 0 0
CUI: C4073063
Disease: Abnormal kinetic perimetry test
Abnormal kinetic perimetry test
4 0 1 5.6E-02 0 0
CUI: C4025715
Disease: Abnormal large intestine morphology
Abnormal large intestine morphology
2 0 1 6.2E-02 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation
32 0 2 4.4E-02 0 0
Abnormal muscle fiber dystrophin expression
1 0 1 6.7E-02 0 0
CUI: C4551596
Disease: Abnormal renal morphology
Abnormal renal morphology
35 0 1 2.0E-02 0 0
Abnormal subcutaneous fat tissue distribution
9 0 2 9.1E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 7.8E-03 0 0
CUI: C4280760
Disease: Abnormal visual accommodation
Abnormal visual accommodation
5 0 1 5.3E-02 0 0
Abnormality of cardiovascular system morphology
198 0 1 4.7E-03 0 0
Abnormality of central sensory function
4 0 1 5.6E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel
96 0 2 1.8E-02 0 0
Abnormality of metabolism/homeostasis
171 0 2 1.1E-02 0 0
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
28 0 1 2.4E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 2 8.8E-03 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum
55 0 3 4.5E-02 0 0