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: C0004245
Disease: Atrioventricular Block
Atrioventricular Block
63 17 3 3.0E-02 1 1.2E-02
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
133 0 5 3.0E-02 0 0
CUI: C0694539
Disease: Chronic atrial fibrillation
Chronic atrial fibrillation
31 0 2 2.9E-02 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
109 220 4 2.7E-02 1 3.5E-03
CUI: C0011989
Disease: Camurati-Engelmann Syndrome
Camurati-Engelmann Syndrome
34 0 2 2.7E-02 0 0
Diastolic blood pressure measurement
35 0 2 2.7E-02 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction
35 0 2 2.7E-02 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular
37 0 2 2.6E-02 0 0
CUI: C0029489
Disease: Other alopecia
Other alopecia
39 0 2 2.6E-02 0 0
CUI: C0039070
Disease: Syncope
Syncope
119 0 4 2.6E-02 0 0
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3
39 0 2 2.6E-02 0 0
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2
39 0 2 2.6E-02 0 0
Left ventricular noncompaction cardiomyopathy
39 0 2 2.6E-02 0 0
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1
39 0 2 2.6E-02 0 0
Alanine aminotransferase measurement
41 0 2 2.5E-02 0 0
Arrhythmogenic Right Ventricular Dysplasia
82 0 3 2.5E-02 0 0
CUI: C0750929
Disease: Arnold-Chiari Malformation, Type I
Arnold-Chiari Malformation, Type I
41 0 2 2.5E-02 0 0
Serum Alanine Aminotransferase Measurement
41 0 2 2.5E-02 0 0
CUI: C0043094
Disease: Weight Gain
Weight Gain
124 0 4 2.5E-02 0 0
CUI: C4021792
Disease: Abnormality of the clavicle
Abnormality of the clavicle
42 0 2 2.5E-02 0 0
CUI: C0007761
Disease: Myoclonic Cerebellar Dyssynergia
Myoclonic Cerebellar Dyssynergia
1 0 1 2.4E-02 0 0
CUI: C0017409
Disease: Herpes Zoster Oticus
Herpes Zoster Oticus
1 0 1 2.4E-02 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis
1 0 1 2.4E-02 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration
1 0 1 2.4E-02 0 0
CUI: C0391816
Disease: Tietz syndrome
Tietz syndrome
1 0 1 2.4E-02 0 0