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: C1833236
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder) 		1 0 1 0.33 0 0
CUI: C1849813
Disease: Glycogen Storage Disease of Heart, Lethal Congenital
Glycogen Storage Disease of Heart, Lethal Congenital 		1 0 1 0.33 0 0
CUI: C1969081
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 12
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 		1 0 1 0.33 0 0
CUI: C2936458
Disease: Fasciculoventricular Accessory Pathway
Fasciculoventricular Accessory Pathway 		1 0 1 0.33 0 0
CUI: C2936459
Disease: Nodoventricular Accessory Pathway
Nodoventricular Accessory Pathway 		1 0 1 0.33 0 0
CUI: C3553060
Disease: EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT 		1 0 1 0.33 0 0
CUI: C4016809
Disease: WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET
WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET 		1 0 1 0.33 0 0
CUI: C4025004
Disease: Ventricular preexcitation with multiple accessory pathways
Ventricular preexcitation with multiple accessory pathways 		1 0 1 0.33 0 0
CUI: C4531287
Disease: Abnormal morphology of right ventricular trabeculae
Abnormal morphology of right ventricular trabeculae 		1 0 1 0.33 0 0
CUI: C0546466
Disease: Idiopathic cardiac hypertrophy
Idiopathic cardiac hypertrophy 		2 0 1 0.25 0 0
CUI: C1864826
Disease: Epidermolysis bullosa, lethal acantholytic
Epidermolysis bullosa, lethal acantholytic 		2 0 1 0.25 0 0
CUI: C3671015
Disease: Myofiber disarray
Myofiber disarray 		2 0 1 0.25 0 0
CUI: C3825246
Disease: Diabetes in old age
Diabetes in old age 		2 0 1 0.25 0 0
CUI: C0151236
Disease: Conduction system abnormalities
Conduction system abnormalities 		3 0 1 0.20 0 0
CUI: C0232347
Disease: No-Reflow Phenomenon
No-Reflow Phenomenon 		3 0 1 0.20 0 0
CUI: C0340420
Disease: Cardiac glycogenosis
Cardiac glycogenosis 		3 0 1 0.20 0 0
CUI: C1858379
Disease: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder) 		3 0 1 0.20 0 0
CUI: C2108093
Disease: continuous electrocardiogram - paroxysmal supraventricular tachycardia
continuous electrocardiogram - paroxysmal supraventricular tachycardia 		3 0 1 0.20 0 0
CUI: C2713615
Disease: Slow-Flow Phenomenon
Slow-Flow Phenomenon 		3 0 1 0.20 0 0
CUI: C0348617
Disease: Other cardiomyopathies
Other cardiomyopathies 		4 0 1 0.17 0 0
CUI: C0520888
Disease: Inverted T wave
Inverted T wave 		4 0 1 0.17 0 0
CUI: C1832600
Disease: Naxos disease
Naxos disease 		4 0 1 0.17 0 0
CUI: C0030590
Disease: Paroxysmal supraventricular tachycardia
Paroxysmal supraventricular tachycardia 		5 0 1 0.14 0 0
CUI: C0455273
Disease: Serum urea measurement
Serum urea measurement 		5 0 1 0.14 0 0
CUI: C0700200
Disease: Presyncope
Presyncope 		5 0 1 0.14 0 0