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: C0340375
Disease: Subaortic stenosis
Subaortic stenosis 		19 2 3 0.11 1 7.1E-02
CUI: C0018808
Disease: Heart murmur
Heart murmur 		31 10 4 0.10 3 0.15
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		10 0 2 1.0E-01 0 0
CUI: C0392482
Disease: Common atrium
Common atrium 		11 1 2 9.5E-02 1 7.7E-02
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 8.3E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 8.3E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 8.3E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 8.3E-02 0 0
CUI: C0431501
Disease: Bilateral arterial duct
Bilateral arterial duct 		1 1 1 8.3E-02 1 7.7E-02
CUI: C0741146
Disease: anxiety acute
anxiety acute 		1 0 1 8.3E-02 0 0
CUI: C1328928
Disease: Multiple Lentigines/LEOPARD syndrome
Multiple Lentigines/LEOPARD syndrome 		1 0 1 8.3E-02 0 0
CUI: C1836050
Disease: Filaminopathy, autosomal dominant
Filaminopathy, autosomal dominant 		1 0 1 8.3E-02 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 0 1 8.3E-02 0 0
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 8.3E-02 0 0
CUI: C1862133
Disease: Decreased finger mobility
Decreased finger mobility 		1 0 1 8.3E-02 0 0
CUI: C2750466
Disease: Cardiomyopathy, Dilated, 1EE
Cardiomyopathy, Dilated, 1EE 		1 0 1 8.3E-02 0 0
CUI: C2750467
Disease: Cardiomyopathy, Familial Hypertrophic, 14
Cardiomyopathy, Familial Hypertrophic, 14 		1 0 1 8.3E-02 0 0
CUI: C3279722
Disease: MYOPATHY, DISTAL, 4
MYOPATHY, DISTAL, 4 		1 0 1 8.3E-02 0 0
CUI: C3279790
Disease: Atrial Septal Defect 3
Atrial Septal Defect 3 		1 0 1 8.3E-02 0 0
CUI: C3279791
Disease: SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO
SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO 		1 0 1 8.3E-02 0 0
CUI: C4014310
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4 		1 7 1 8.3E-02 1 5.3E-02
CUI: C4016662
Disease: ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 8.3E-02 0 0
CUI: C4016663
Disease: ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 8.3E-02 0 0
CUI: C4017089
Disease: LONG QT SYNDROME 1, RECESSIVE
LONG QT SYNDROME 1, RECESSIVE 		1 0 1 8.3E-02 0 0
CUI: C4021943
Disease: Abnormality of the xiphoid process
Abnormality of the xiphoid process 		1 1 1 8.3E-02 1 7.7E-02