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: C2750466
Disease: Cardiomyopathy, Dilated, 1EE
Cardiomyopathy, Dilated, 1EE 		1 0 1 0.33 0 0
CUI: C2750467
Disease: Cardiomyopathy, Familial Hypertrophic, 14
Cardiomyopathy, Familial Hypertrophic, 14 		1 0 1 0.33 0 0
CUI: C3279790
Disease: Atrial Septal Defect 3
Atrial Septal Defect 3 		1 0 1 0.33 0 0
CUI: C3279791
Disease: SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO
SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO 		1 0 1 0.33 0 0
CUI: C3805326
Disease: Congenital heart disease (variable)
Congenital heart disease (variable) 		1 0 1 0.33 0 0
CUI: C0265239
Disease: Wildervanck's syndrome
Wildervanck's syndrome 		2 0 1 0.25 0 0
CUI: C0265559
Disease: Acheiropodia
Acheiropodia 		2 0 1 0.25 0 0
CUI: C1868705
Disease: Shone complex
Shone complex 		2 0 1 0.25 0 0
CUI: C3542024
Disease: AORTIC VALVE DISEASE 2
AORTIC VALVE DISEASE 2 		2 0 1 0.25 0 0
CUI: C0340491
Disease: Familial sick sinus syndrome
Familial sick sinus syndrome 		3 0 1 0.20 0 0
CUI: C0344730
Disease: Atrial Septal Defect Sinus Venosus
Atrial Septal Defect Sinus Venosus 		3 0 1 0.20 0 0
CUI: C0429021
Disease: P wave duration (observable entity)
P wave duration (observable entity) 		10 0 2 0.18 0 0
CUI: C0265246
Disease: Townes syndrome
Townes syndrome 		4 0 1 0.17 0 0
CUI: C4023124
Disease: Short digit
Short digit 		4 0 1 0.17 0 0
CUI: C0751605
Disease: X-Linked, Spastic Paraplegia, Hereditary
X-Linked, Spastic Paraplegia, Hereditary 		5 0 1 0.14 0 0
CUI: C3241958
Disease: Myocardial Disorder
Myocardial Disorder 		5 0 1 0.14 0 0
CUI: C3874346
Disease: Skeletal malocclusion
Skeletal malocclusion 		5 0 1 0.14 0 0
CUI: C4024213
Disease: Aplasia of the pectoralis major muscle
Aplasia of the pectoralis major muscle 		5 0 1 0.14 0 0
CUI: C0031538
Disease: Phimosis
Phimosis 		6 0 1 0.12 0 0
CUI: C0576227
Disease: Narrow foot
Narrow foot 		6 0 1 0.12 0 0
CUI: C1840535
Disease: Abnormality of the carpal bones
Abnormality of the carpal bones 		6 0 1 0.12 0 0
CUI: C1846474
Disease: Small thenar eminence
Small thenar eminence 		6 0 1 0.12 0 0
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 1 0.11 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 1 0.11 0 0
CUI: C0796225
Disease: Mental Retardation, X-Linked 19
Mental Retardation, X-Linked 19 		7 0 1 0.11 0 0