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: C0018810
Disease: heart rate
heart rate 		0 103 0 0 1 7.8E-03
CUI: C0007761
Disease: Myoclonic Cerebellar Dyssynergia
Myoclonic Cerebellar Dyssynergia 		1 0 1 5.9E-02 0 0
CUI: C0017409
Disease: Herpes Zoster Oticus
Herpes Zoster Oticus 		1 0 1 5.9E-02 0 0
CUI: C0685108
Disease: Lenegre's disease
Lenegre's disease 		1 0 1 5.9E-02 0 0
CUI: C0748694
Disease: sick sinus
sick sinus 		1 0 1 5.9E-02 0 0
CUI: C0856322
Disease: Alcoholic brain damage
Alcoholic brain damage 		1 0 1 5.9E-02 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 5.9E-02 0 0
CUI: C1834580
Disease: MYOCLONUS AND ATAXIA
MYOCLONUS AND ATAXIA 		1 0 1 5.9E-02 0 0
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding) 		1 0 1 5.9E-02 0 0
CUI: C1849307
Disease: Increased density of long bones
Increased density of long bones 		1 0 1 5.9E-02 0 0
CUI: C1849309
Disease: Wide distal femoral metaphysis
Wide distal femoral metaphysis 		1 0 1 5.9E-02 0 0
CUI: C1861983
Disease: Heart Block, Nonprogressive
Heart Block, Nonprogressive 		1 0 1 5.9E-02 0 0
CUI: C1861984
Disease: Cardiac Conduction Defect, Nonprogressive
Cardiac Conduction Defect, Nonprogressive 		1 0 1 5.9E-02 0 0
CUI: C2114320
Disease: preterm contractions
preterm contractions 		1 0 1 5.9E-02 0 0
CUI: C2216002
Disease: electrocardiogram left posterior hemiblock (finding)
electrocardiogram left posterior hemiblock (finding) 		1 0 1 5.9E-02 0 0
CUI: C2930805
Disease: Sudden unexpected nocturnal death syndrome
Sudden unexpected nocturnal death syndrome 		1 0 1 5.9E-02 0 0
CUI: C3151036
Disease: CHROMOSOME 1p32-p31 DELETION SYNDROME
CHROMOSOME 1p32-p31 DELETION SYNDROME 		1 0 1 5.9E-02 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 0 1 5.9E-02 0 0
CUI: C3279627
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC, 6
EPILEPSY, PROGRESSIVE MYOCLONIC, 6 		1 0 1 5.9E-02 0 0
CUI: C3805326
Disease: Congenital heart disease (variable)
Congenital heart disease (variable) 		1 0 1 5.9E-02 0 0
CUI: C3809893
Disease: EPISODIC PAIN SYNDROME, FAMILIAL, 2
EPISODIC PAIN SYNDROME, FAMILIAL, 2 		1 0 1 5.9E-02 0 0
CUI: C3814825
Disease: Sudden Unexplained Infant Death
Sudden Unexplained Infant Death 		1 0 1 5.9E-02 0 0
CUI: C4015141
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 29
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 		1 0 1 5.9E-02 0 0
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC 		1 0 1 5.9E-02 0 0
CUI: C4021532
Disease: Abnormality of the stapes
Abnormality of the stapes 		1 0 1 5.9E-02 0 0