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: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 3.3E-02 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 10 1 3.3E-02 1 1.6E-02
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding) 		1 0 1 3.3E-02 0 0
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 3.3E-02 0 0
CUI: C1844615
Disease: Skin peeling/scaling (newborn)
Skin peeling/scaling (newborn) 		1 0 1 3.3E-02 0 0
CUI: C1844617
Disease: Hypoplastic-absent sebaceous glands
Hypoplastic-absent sebaceous glands 		1 0 1 3.3E-02 0 0
CUI: C1853701
Disease: Muscle hyperirritability
Muscle hyperirritability 		1 0 1 3.3E-02 0 0
CUI: C1861983
Disease: Heart Block, Nonprogressive
Heart Block, Nonprogressive 		1 0 1 3.3E-02 0 0
CUI: C1861984
Disease: Cardiac Conduction Defect, Nonprogressive
Cardiac Conduction Defect, Nonprogressive 		1 0 1 3.3E-02 0 0
CUI: C1862394
Disease: Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 4 		1 0 1 3.3E-02 0 0
CUI: C1867904
Disease: LONG QT SYNDROME 5
LONG QT SYNDROME 5 		1 21 1 3.3E-02 2 2.7E-02
CUI: C1970757
Disease: Tooth Agenesis, Selective, X-Linked, 1
Tooth Agenesis, Selective, X-Linked, 1 		1 0 1 3.3E-02 0 0
CUI: C1998313
Disease: T wave alternans
T wave alternans 		1 0 1 3.3E-02 0 0
CUI: C2063886
Disease: Esophageal Adenosquamous Carcinoma
Esophageal Adenosquamous Carcinoma 		1 0 1 3.3E-02 0 0
CUI: C2114320
Disease: preterm contractions
preterm contractions 		1 0 1 3.3E-02 0 0
CUI: C2216002
Disease: electrocardiogram left posterior hemiblock (finding)
electrocardiogram left posterior hemiblock (finding) 		1 0 1 3.3E-02 0 0
CUI: C2675237
Disease: Deafness, Autosomal Dominant 3B
Deafness, Autosomal Dominant 3B 		1 0 1 3.3E-02 0 0
CUI: C2676723
Disease: JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)
JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder) 		1 7 1 3.3E-02 1 1.7E-02
CUI: C2677106
Disease: Atrial Fibrillation, Familial, 7
Atrial Fibrillation, Familial, 7 		1 0 1 3.3E-02 0 0
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		1 0 1 3.3E-02 0 0
CUI: C2678483
Disease: Long Qt Syndrome 11
Long Qt Syndrome 11 		1 0 1 3.3E-02 0 0
CUI: C2678484
Disease: Long Qt Syndrome 10
Long Qt Syndrome 10 		1 3 1 3.3E-02 1 1.8E-02
CUI: C2751830
Disease: Long Qt Syndrome 12
Long Qt Syndrome 12 		1 2 1 3.3E-02 1 1.8E-02
CUI: C2930805
Disease: Sudden unexpected nocturnal death syndrome
Sudden unexpected nocturnal death syndrome 		1 0 1 3.3E-02 0 0
CUI: C2930879
Disease: Cerebellar degeneration, subacute
Cerebellar degeneration, subacute 		1 0 1 3.3E-02 0 0