Source: ALL
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: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 4 0.33 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 4 0.33 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 7 0.22 0 0
CUI: C0340375
Disease: Subaortic stenosis
Subaortic stenosis 		19 0 4 0.17 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 0 4 0.15 0 0
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy 		31 7 5 0.14 1 5.9E-03
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		8 0 2 0.13 0 0
CUI: C0410198
Disease: Proximal myopathy
Proximal myopathy 		8 0 2 0.13 0 0
CUI: C2748884
Disease: CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC 		9 0 2 0.12 0 0
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy 		10 0 2 0.12 0 0
CUI: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 0.11 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 0.11 0 0
CUI: C0878565
Disease: Electrocardiogram J wave
Electrocardiogram J wave 		1 0 1 0.11 0 0
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
CARDIOMYOPATHY, DILATED, 1D (disorder) 		1 24 1 0.11 1 5.4E-03
CUI: C1837471
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8 		1 8 1 0.11 1 5.9E-03
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 11 1 0.11 10 6.1E-02
CUI: C1853701
Disease: Muscle hyperirritability
Muscle hyperirritability 		1 0 1 0.11 0 0
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
Cardiomyopathy, Familial Hypertrophic, 2 		1 30 1 0.11 1 5.2E-03
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder) 		1 21 1 0.11 1 5.5E-03
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		1 0 1 0.11 0 0
CUI: C2750466
Disease: Cardiomyopathy, Dilated, 1EE
Cardiomyopathy, Dilated, 1EE 		1 0 1 0.11 0 0
CUI: C2750467
Disease: Cardiomyopathy, Familial Hypertrophic, 14
Cardiomyopathy, Familial Hypertrophic, 14 		1 0 1 0.11 0 0
CUI: C2751427
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO 		1 0 1 0.11 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly 		1 0 1 0.11 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5 		1 6 1 0.11 2 1.2E-02