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: C0001925
Disease: Albuminuria
Albuminuria 		76 0 1 1.3E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 0 1 2.4E-02 0 0
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia 		52 0 1 1.9E-02 0 0
CUI: C0018801
Disease: Heart failure
Heart failure 		1499 0 1 6.7E-04 0 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		1760 0 1 5.7E-04 0 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		2322 0 1 4.3E-04 0 0
CUI: C0030252
Disease: Palpitations
Palpitations 		70 0 1 1.4E-02 0 0
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		96 0 1 1.0E-02 0 0
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death 		133 0 1 7.5E-03 0 0
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		403 0 1 2.5E-03 0 0
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		267 0 1 3.7E-03 0 0
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		766 0 1 1.3E-03 0 0
CUI: C0231807
Disease: Dyspnea on exertion
Dyspnea on exertion 		102 0 1 9.8E-03 0 0
CUI: C0232310
Disease: P mitrale (finding)
P mitrale (finding) 		3 0 1 0.33 0 0
CUI: C0238705
Disease: Left atrial hypertrophy
Left atrial hypertrophy 		3 0 1 0.33 0 0
CUI: C0266258
Disease: Congenital absence of liver
Congenital absence of liver 		25 0 1 4.0E-02 0 0
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		254 0 1 3.9E-03 0 0
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		507 0 1 2.0E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		146 0 1 6.8E-03 0 0
CUI: C0520888
Disease: Inverted T wave
Inverted T wave 		4 0 1 0.25 0 0
CUI: C0553980
Disease: Endomyocardial Fibrosis
Endomyocardial Fibrosis 		20 0 1 5.0E-02 0 0
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		6776 0 1 1.5E-04 0 0
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		30 0 1 3.3E-02 0 0
CUI: C0751951
Disease: Central Core Myopathy (disorder)
Central Core Myopathy (disorder) 		44 0 1 2.3E-02 0 0
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		773 0 1 1.3E-03 0 0