Source: CLINVAR ×
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: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		2 0 1 2.3E-02 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 9 1 2.3E-02 1 2.2E-03
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter 		2 0 2 4.7E-02 0 0
CUI: C4023223
Disease: Atrial reentry tachycardia
Atrial reentry tachycardia 		2 0 2 4.7E-02 0 0
CUI: C1862389
Disease: ATRIAL SEPTAL DEFECT 1
ATRIAL SEPTAL DEFECT 1 		3 0 1 2.2E-02 0 0
CUI: C2748552
Disease: Atrial Septal Defect 5
Atrial Septal Defect 5 		1 0 1 2.3E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		37 43 3 3.9E-02 1 2.1E-03
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC 		1 0 1 2.3E-02 0 0
CUI: C0162154
Disease: Atrophic scar
Atrophic scar 		2 3 1 2.3E-02 1 2.2E-03
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 25 1 2.3E-02 5 1.1E-02
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		1 0 1 2.3E-02 0 0
CUI: C0149630
Disease: Bicuspid aortic valve
Bicuspid aortic valve 		7 0 1 2.0E-02 0 0
CUI: C1865916
Disease: Bilateral ptosis
Bilateral ptosis 		11 0 2 3.8E-02 0 0
CUI: C0281788
Disease: Biventricular hypertrophy
Biventricular hypertrophy 		3 0 2 4.5E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 49 2 2.6E-02 1 2.0E-03
CUI: C4692845
Disease: BLEPHAROSPASM, BENIGN ESSENTIAL, SUSCEPTIBILITY TO
BLEPHAROSPASM, BENIGN ESSENTIAL, SUSCEPTIBILITY TO 		2 2 1 2.3E-02 1 2.3E-03
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 2.3E-02 0 0
CUI: C0856863
Disease: Broad-based gait
Broad-based gait 		19 0 3 5.1E-02 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		3 103 1 2.2E-02 3 5.5E-03
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		1 34 1 2.3E-02 1 2.1E-03
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots 		18 32 1 1.7E-02 1 2.1E-03
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		2 5 1 2.3E-02 1 2.2E-03
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		4 3 3 6.8E-02 1 2.2E-03
CUI: C1861984
Disease: Cardiac Conduction Defect, Nonprogressive
Cardiac Conduction Defect, Nonprogressive 		1 0 1 2.3E-02 0 0
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		3 0 2 4.5E-02 0 0