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: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa 		201 661 1 5.0E-03 2 2.9E-03
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		560 635 1 1.8E-03 16 2.5E-02
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		512 509 1 2.0E-03 6 1.1E-02
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		83 355 1 1.2E-02 6 1.6E-02
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		925 294 1 1.1E-03 4 1.3E-02
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		773 243 1 1.3E-03 3 1.1E-02
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 163 1 0.11 1 5.2E-03
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0 96 0 0 1 8.0E-03
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
Hypertrophic obstructive cardiomyopathy 		233 90 1 4.3E-03 4 3.4E-02
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 30 1 2.4E-02 2 3.4E-02
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
CARDIOMYOPATHY, DILATED, 1D (disorder) 		1 24 1 1.00 22 0.69
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder) 		1 21 1 1.00 21 0.70
CUI: C0442887
Disease: Septal hypertrophy
Septal hypertrophy 		0 11 0 0 1 2.5E-02
CUI: C3825201
Disease: Mitochondrial pathology
Mitochondrial pathology 		0 6 0 0 1 2.9E-02
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		234 0 1 4.3E-03 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		559 0 1 1.8E-03 0 0
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		2044 0 1 4.9E-04 0 0
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		1756 0 1 5.7E-04 0 0
CUI: C0008031
Disease: Chest Pain
Chest Pain 		154 0 1 6.5E-03 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 1 3.3E-02 0 0
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		766 0 1 1.3E-03 0 0
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia 		88 0 1 1.1E-02 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		194 0 1 5.2E-03 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 0 1 1.3E-03 0 0
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		537 0 1 1.9E-03 0 0