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: C2677794
Disease: Stress-induced polymorphic ventricular tachycardia
Stress-induced polymorphic ventricular tachycardia 		5 0 4 0.57 0 0
CUI: C0751534
Disease: Syncopal Episode
Syncopal Episode 		7 0 2 0.18 0 0
CUI: C0235242
Disease: Syncope, Effort
Syncope, Effort 		1 0 1 0.17 0 0
CUI: C1386553
Disease: Caffeine dependence
Caffeine dependence 		1 0 1 0.17 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 0.17 0 0
CUI: C1861753
Disease: Multiminicore Disease, Moderate, with Hand Involvement
Multiminicore Disease, Moderate, with Hand Involvement 		1 0 1 0.17 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy 		1 0 1 0.17 0 0
CUI: C2674259
Disease: NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) 		1 0 1 0.17 0 0
CUI: C2677105
Disease: Inflammatory Bowel Disease 12
Inflammatory Bowel Disease 12 		1 0 1 0.17 0 0
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		1 0 1 0.17 0 0
CUI: C3151463
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 		1 0 1 0.17 0 0
CUI: C3554047
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4 		1 0 1 0.17 0 0
CUI: C4015671
Disease: LONG QT SYNDROME 14
LONG QT SYNDROME 14 		1 0 1 0.17 0 0
CUI: C4016143
Disease: VENTRICULAR TACHYCARDIA, SOMATIC
VENTRICULAR TACHYCARDIA, SOMATIC 		1 0 1 0.17 0 0
CUI: C4016368
Disease: CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE
CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE 		1 0 1 0.17 0 0
CUI: C4476998
Disease: Frog-leg posture
Frog-leg posture 		1 0 1 0.17 0 0
CUI: C4706390
Disease: Congenital myopathy with myasthenic-like onset
Congenital myopathy with myasthenic-like onset 		1 0 1 0.17 0 0
CUI: C4749502
Disease: Benign Samaritan congenital myopathy
Benign Samaritan congenital myopathy 		1 0 1 0.17 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 5 0.16 0 0
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		31 0 5 0.16 0 0
CUI: C0155338
Disease: Total ophthalmoplegia
Total ophthalmoplegia 		2 0 1 0.14 0 0
CUI: C0263992
Disease: Exertional rhabdomyolysis (disorder)
Exertional rhabdomyolysis (disorder) 		2 0 1 0.14 0 0
CUI: C1963282
Disease: Wolff-Parkinson-White Syndrome, CTCAE
Wolff-Parkinson-White Syndrome, CTCAE 		2 0 1 0.14 0 0
CUI: C2930902
Disease: Bidirectional tachycardia
Bidirectional tachycardia 		2 0 1 0.14 0 0
CUI: C4016392
Disease: ADRENOCORTICAL TUMOR, SOMATIC
ADRENOCORTICAL TUMOR, SOMATIC 		2 0 1 0.14 0 0