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: 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: C0751172
Disease: Adult Glycogen Storage Disease Type II
Adult Glycogen Storage Disease Type II 		2 0 1 0.50 0 0
CUI: C0751174
Disease: Glycogen Storage Disease Type II, Juvenile
Glycogen Storage Disease Type II, Juvenile 		2 0 1 0.50 0 0
CUI: C1841658
Disease: Progressive Familial Heart Block, Type II
Progressive Familial Heart Block, Type II 		2 0 1 0.50 0 0
CUI: C0751173
Disease: Glycogen Storage Disease Type II, Infantile
Glycogen Storage Disease Type II, Infantile 		4 0 1 0.25 0 0
CUI: C0348616
Disease: Other restrictive cardiomyopathy
Other restrictive cardiomyopathy 		5 0 1 0.20 0 0
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 1 0.14 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 1 0.14 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 163 1 0.11 1 5.2E-03
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		11 0 1 9.1E-02 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 0 1 4.8E-02 0 0
CUI: C1720824
Disease: Sudden Cardiac Arrest
Sudden Cardiac Arrest 		27 0 1 3.7E-02 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 1 3.3E-02 0 0
CUI: C1527303
Disease: Chronic Airflow Obstruction
Chronic Airflow Obstruction 		35 0 1 2.9E-02 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		35 0 1 2.9E-02 0 0
CUI: C4551854
Disease: HYPOPLASTIC LEFT HEART SYNDROME 1
HYPOPLASTIC LEFT HEART SYNDROME 1 		37 0 1 2.7E-02 0 0
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		39 0 1 2.6E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 30 1 2.4E-02 2 3.4E-02
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		41 0 1 2.4E-02 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		48 0 1 2.1E-02 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 1 2.0E-02 0 0
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 0 1 1.9E-02 0 0
CUI: C0027540
Disease: Necrosis
Necrosis 		60 0 1 1.7E-02 0 0
CUI: C0340279
Disease: Ventricular hypertrophy
Ventricular hypertrophy 		60 0 1 1.7E-02 0 0