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: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne
1 0 1 2.3E-02 0 0
CUI: C0018794
Disease: Heart Block
Heart Block
1 0 1 2.3E-02 0 0
CUI: C0023211
Disease: Left Bundle-Branch Block
Left Bundle-Branch Block
1 0 1 2.3E-02 0 0
Paroxysmal supraventricular tachycardia
1 0 1 2.3E-02 0 0
CUI: C0033300
Disease: Progeria
Progeria
1 20 1 2.3E-02 2 4.3E-03
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome
1 0 1 2.3E-02 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder)
1 0 1 2.3E-02 0 0
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy
1 0 1 2.3E-02 0 0
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis
1 1 1 2.3E-02 1 2.3E-03
CUI: C0239574
Disease: Low grade fever
Low grade fever
1 0 1 2.3E-02 0 0
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart
1 0 1 2.3E-02 0 0
Second degree atrioventricular block
1 0 1 2.3E-02 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
1 0 1 2.3E-02 0 0
Pulmonary Atresia with Intact Ventricular Septum
1 0 1 2.3E-02 0 0
Disorders of both mitral and tricuspid valves
1 0 1 2.3E-02 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma
1 0 1 2.3E-02 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
1 0 1 2.3E-02 0 0
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
1 25 1 2.3E-02 5 1.1E-02
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder)
1 0 1 2.3E-02 0 0
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
1 8 1 2.3E-02 1 2.2E-03
CUI: C0476369
Disease: Echocardiogram abnormal
Echocardiogram abnormal
1 1 1 2.3E-02 1 2.3E-03
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
1 22 1 2.3E-02 5 1.1E-02
CUI: C0750929
Disease: Arnold-Chiari Malformation, Type I
Arnold-Chiari Malformation, Type I
1 0 1 2.3E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
1 4 1 2.3E-02 1 2.2E-03
CUI: C0878677
Disease: Glycogen Storage Disease Type IIb
Glycogen Storage Disease Type IIb
1 37 1 2.3E-02 1 2.1E-03