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: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature 		2 0 1 0.25 0 0
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris 		2 0 1 0.25 0 0
CUI: C0349788
Disease: Arrhythmogenic Right Ventricular Dysplasia
Arrhythmogenic Right Ventricular Dysplasia 		11 0 1 7.7E-02 0 0
CUI: C1836906
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 		5 0 1 0.14 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		16 0 1 5.6E-02 0 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		2 0 1 0.25 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 0 1 0.33 0 0
CUI: C3809311
Disease: ATRIAL FIBRILLATION, FAMILIAL, 13
ATRIAL FIBRILLATION, FAMILIAL, 13 		1 0 1 0.33 0 0
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC 		1 0 1 0.33 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 0 1 0.33 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 0.33 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		3 103 1 0.20 1 9.4E-03
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		1 34 1 0.33 1 2.7E-02
CUI: C2748541
Disease: Brugada Syndrome 5
Brugada Syndrome 5 		1 0 1 0.33 0 0
CUI: C1861984
Disease: Cardiac Conduction Defect, Nonprogressive
Cardiac Conduction Defect, Nonprogressive 		1 0 1 0.33 0 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		45 0 2 4.3E-02 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		43 0 2 4.5E-02 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 0.33 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 0 1 9.1E-02 0 0
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		4 0 1 0.17 0 0
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		24 0 1 3.8E-02 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		24 0 1 3.8E-02 0 0
CUI: C1854154
Disease: Charcot-Marie-Tooth disease, Type 2B1
Charcot-Marie-Tooth disease, Type 2B1 		3 0 1 0.20 0 0
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome 		5 0 1 0.14 0 0
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		12 0 1 7.1E-02 0 0