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: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart
41 0 1 2.4E-02 0 0
Congenital muscular dystrophy (disorder)
54 0 1 1.9E-02 0 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
1760 0 1 5.7E-04 0 0
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
1708 0 1 5.9E-04 0 0
Creatine phosphokinase serum increased
228 0 1 4.4E-03 0 0
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
766 0 1 1.3E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 1 7.7E-03 0 0
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
1075 0 1 9.3E-04 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
83 0 1 1.2E-02 0 0
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia
88 0 1 1.1E-02 0 0
Generalized glycogen storage disease of infants
51 0 1 2.0E-02 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
194 0 1 5.2E-03 0 0
Glycogen Storage Disease Type II, Infantile
4 0 1 0.25 0 0
Glycogen Storage Disease Type II, Juvenile
2 0 1 0.50 0 0
CUI: C1961112
Disease: Heart Decompensation
Heart Decompensation
113 0 1 8.8E-03 0 0
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
537 0 1 1.9E-03 0 0
CUI: C0018801
Disease: Heart failure
Heart failure
1499 0 1 6.7E-04 0 0
CUI: C0235527
Disease: Heart Failure, Right-Sided
Heart Failure, Right-Sided
154 0 1 6.5E-03 0 0
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa
201 661 1 5.0E-03 2 2.9E-03
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
560 635 1 1.8E-03 16 2.5E-02
Hypertrophic obstructive cardiomyopathy
233 90 1 4.3E-03 4 3.4E-02
CUI: C4551854
Disease: HYPOPLASTIC LEFT HEART SYNDROME 1
HYPOPLASTIC LEFT HEART SYNDROME 1
37 0 1 2.7E-02 0 0
Idiopathic hypertrophic subaortic stenosis
7 0 1 0.14 0 0
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
1630 0 1 6.1E-04 0 0
CUI: C4551675
Disease: Keratoderma, Palmoplantar
Keratoderma, Palmoplantar
165 0 1 6.1E-03 0 0