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: C0003886
Disease: Arthrogryposis
Arthrogryposis
16 0 3 6.0E-02 0 0
CUI: C0005697
Disease: Neurogenic Urinary Bladder
Neurogenic Urinary Bladder
7 0 1 2.3E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
37 0 3 4.2E-02 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation
10 0 1 2.2E-02 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
43 0 5 6.7E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy
6 0 1 2.4E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
44 0 1 1.3E-02 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
24 0 3 5.2E-02 0 0
CUI: C0008031
Disease: Chest Pain
Chest Pain
4 0 1 2.5E-02 0 0
CUI: C0008370
Disease: Cholestasis
Cholestasis
4 0 1 2.5E-02 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
26 0 1 1.6E-02 0 0
CUI: C0009806
Disease: Constipation
Constipation
40 0 3 4.1E-02 0 0
CUI: C0013132
Disease: Drooling
Drooling
14 0 1 2.0E-02 0 0
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne
1 0 1 2.7E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
34 0 1 1.4E-02 0 0
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly
2 0 1 2.6E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
33 0 1 1.4E-02 0 0
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
7 0 1 2.3E-02 0 0
CUI: C0015310
Disease: Exotropia
Exotropia
17 0 1 1.9E-02 0 0
CUI: C0015672
Disease: Fatigue
Fatigue
18 0 1 1.9E-02 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence
10 0 1 2.2E-02 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
30 0 1 1.5E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent
11 0 1 2.1E-02 0 0
Hereditary fructose intolerance syndrome
2 0 1 2.6E-02 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
26 0 1 1.6E-02 0 0