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: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 5.6E-02 0 0
CUI: C0235242
Disease: Syncope, Effort
Syncope, Effort 		1 0 1 5.6E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 5.6E-02 0 0
CUI: C0543816
Disease: Progressive cardiomyopathic lentiginosis syndrome
Progressive cardiomyopathic lentiginosis syndrome 		1 0 1 5.6E-02 0 0
CUI: C0685108
Disease: Lenegre's disease
Lenegre's disease 		1 0 1 5.6E-02 0 0
CUI: C0748694
Disease: sick sinus
sick sinus 		1 0 1 5.6E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 5.6E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 5.6E-02 0 0
CUI: C0878565
Disease: Electrocardiogram J wave
Electrocardiogram J wave 		1 0 1 5.6E-02 0 0
CUI: C1386553
Disease: Caffeine dependence
Caffeine dependence 		1 0 1 5.6E-02 0 0
CUI: C1739133
Disease: Mucocutaneous herpes simplex
Mucocutaneous herpes simplex 		1 0 1 5.6E-02 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 5.6E-02 0 0
CUI: C1833154
Disease: Long Qt Syndrome 4
Long Qt Syndrome 4 		1 0 1 5.6E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 5.6E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 5.6E-02 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 0 1 5.6E-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 5.6E-02 0 0
CUI: C1843292
Disease: Skin Fragility-Woolly Hair Syndrome
Skin Fragility-Woolly Hair Syndrome 		1 0 1 5.6E-02 0 0
CUI: C1843294
Disease: Palmoplantar keratosis with erythema and scale
Palmoplantar keratosis with erythema and scale 		1 0 1 5.6E-02 0 0
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 5.6E-02 0 0
CUI: C1843896
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 		1 0 1 5.6E-02 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 5.6E-02 0 0
CUI: C1852127
Disease: KERATOSIS PALMOPLANTARIS STRIATA II
KERATOSIS PALMOPLANTARIS STRIATA II 		1 0 1 5.6E-02 0 0
CUI: C1854063
Disease: Cardiomyopathy dilated with Woolly hair and keratoderma
Cardiomyopathy dilated with Woolly hair and keratoderma 		1 0 1 5.6E-02 0 0
CUI: C1856888
Disease: Clinodactyly of the thumb
Clinodactyly of the thumb 		1 1 1 5.6E-02 1 3.7E-02