Source: CLINVAR ×
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: C2751427
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO 		1 0 1 0.14 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5 		1 6 1 0.14 2 2.1E-02
CUI: C3279790
Disease: Atrial Septal Defect 3
Atrial Septal Defect 3 		1 0 1 0.14 0 0
CUI: C3279791
Disease: SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO
SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO 		1 0 1 0.14 0 0
CUI: C3552821
Disease: EEG with photoparoxysmal response
EEG with photoparoxysmal response 		1 0 1 0.14 0 0
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
LEFT VENTRICULAR NONCOMPACTION 10 		1 18 1 0.14 1 9.1E-03
CUI: C4016270
Disease: CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC
CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC 		1 0 1 0.14 0 0
CUI: C4476545
Disease: Dilatation of the ventricular cavity
Dilatation of the ventricular cavity 		1 0 1 0.14 0 0
CUI: C4552004
Disease: Distal Myopathy 1
Distal Myopathy 1 		1 35 1 0.14 11 9.4E-02
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		29 468 4 0.12 53 0.10
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		2 0 1 0.12 0 0
CUI: C0751337
Disease: X-Linked Emery-Dreifuss Muscular Dystrophy
X-Linked Emery-Dreifuss Muscular Dystrophy 		2 33 1 0.12 11 9.6E-02
CUI: C1963282
Disease: Wolff-Parkinson-White Syndrome, CTCAE
Wolff-Parkinson-White Syndrome, CTCAE 		2 0 1 0.12 0 0
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		3 0 1 0.11 0 0
CUI: C0085636
Disease: Photophobia
Photophobia 		3 0 1 0.11 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		3 0 1 0.11 0 0
CUI: C1849683
Disease: No social interaction
No social interaction 		3 0 1 0.11 0 0
CUI: C1861862
Disease: Familial Hypertrophic Cardiomyopathy Type 4
Familial Hypertrophic Cardiomyopathy Type 4 		3 96 1 0.11 4 2.2E-02
CUI: C4021734
Disease: Abnormality of mitochondrial metabolism
Abnormality of mitochondrial metabolism 		3 0 1 0.11 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		3 0 1 0.11 0 0
CUI: C0008031
Disease: Chest Pain
Chest Pain 		4 5 1 1.0E-01 1 1.0E-02
CUI: C0011071
Disease: Sudden death
Sudden death 		4 0 1 1.0E-01 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		4 0 1 1.0E-01 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance 		4 0 1 1.0E-01 0 0
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		4 0 1 1.0E-01 0 0