Source: CLINVAR ×
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: C1836906
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 		5 61 3 0.23 21 0.14
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 		2 27 2 0.18 5 3.8E-02
CUI: C2752072
Disease: Cardiomyopathy, Dilated, 1BB
Cardiomyopathy, Dilated, 1BB 		2 0 2 0.18 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 0 3 0.18 0 0
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		3 4 2 0.17 2 1.8E-02
CUI: C2063326
Disease: Right ventricular cardiomyopathy
Right ventricular cardiomyopathy 		4 0 2 0.15 0 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		45 172 7 0.14 6 2.2E-02
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		43 443 6 0.12 14 2.6E-02
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		8 0 2 0.12 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change 		18 27 3 0.12 4 3.1E-02
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases 		11 0 2 1.0E-01 0 0
CUI: C0023211
Disease: Left Bundle-Branch Block
Left Bundle-Branch Block 		1 0 1 9.1E-02 0 0
CUI: C0030590
Disease: Paroxysmal supraventricular tachycardia
Paroxysmal supraventricular tachycardia 		1 0 1 9.1E-02 0 0
CUI: C0033300
Disease: Progeria
Progeria 		1 20 1 9.1E-02 1 7.9E-03
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 9.1E-02 0 0
CUI: C0264906
Disease: Second degree atrioventricular block
Second degree atrioventricular block 		1 0 1 9.1E-02 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		1 0 1 9.1E-02 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		1 0 1 9.1E-02 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 25 1 9.1E-02 1 7.6E-03
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		1 8 1 9.1E-02 1 8.7E-03
CUI: C0520806
Disease: Unexplained sudden death
Unexplained sudden death 		1 0 1 9.1E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 4 1 9.1E-02 1 9.0E-03
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		1 17 1 9.1E-02 1 8.1E-03
CUI: C1832370
Disease: MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED 		1 0 1 9.1E-02 0 0
CUI: C1832600
Disease: Naxos disease
Naxos disease 		1 7 1 9.1E-02 1 8.8E-03