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 0.31 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 4 0.31 0 0
CUI: C4477072
Disease: Iris flocculi
Iris flocculi 		2 0 2 0.20 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 0 5 0.19 0 0
CUI: C4324548
Disease: Non-compaction cardiomyopathy
Non-compaction cardiomyopathy 		9 0 3 0.19 0 0
CUI: C0014040
Disease: Encephalitis Lethargica
Encephalitis Lethargica 		3 0 2 0.18 0 0
CUI: C0751656
Disease: Nemaline Myopathy, Autosomal Dominant
Nemaline Myopathy, Autosomal Dominant 		4 0 2 0.17 0 0
CUI: C3151201
Disease: MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME 		4 0 2 0.17 0 0
CUI: C0877854
Disease: Cerebral Arteriosclerosis
Cerebral Arteriosclerosis 		5 0 2 0.15 0 0
CUI: C0751657
Disease: Nemaline Myopathy, Autosomal Recessive
Nemaline Myopathy, Autosomal Recessive 		7 0 2 0.13 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		7 0 2 0.13 0 0
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		8 0 2 0.12 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		35 0 5 0.12 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 0 2 0.12 0 0
CUI: C2748884
Disease: CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC 		9 0 2 0.12 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 0 2 0.12 0 0
CUI: C3710589
Disease: Cap Myopathy
Cap Myopathy 		9 0 2 0.12 0 0
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		10 0 2 0.11 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 1.0E-01 0 0
CUI: C0006915
Disease: Caplan Syndrome
Caplan Syndrome 		1 0 1 1.0E-01 0 0
CUI: C0007462
Disease: Causalgia
Causalgia 		1 0 1 1.0E-01 0 0
CUI: C0024588
Disease: Malignant essential hypertension
Malignant essential hypertension 		1 0 1 1.0E-01 0 0
CUI: C0032298
Disease: Pneumonia, Lipid
Pneumonia, Lipid 		1 0 1 1.0E-01 0 0
CUI: C0040213
Disease: Tietze's Syndrome
Tietze's Syndrome 		1 0 1 1.0E-01 0 0
CUI: C0153445
Disease: Malignant neoplasm of anal canal
Malignant neoplasm of anal canal 		1 0 1 1.0E-01 0 0