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: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 30 12 0.24 12 0.29
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 5 0.22 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 5 0.22 0 0
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy 		10 0 5 0.19 0 0
CUI: C0348616
Disease: Other restrictive cardiomyopathy
Other restrictive cardiomyopathy 		5 0 4 0.18 0 0
CUI: C1333500
Disease: Extragastrointestinal Gastrointestinal Stromal Tumor
Extragastrointestinal Gastrointestinal Stromal Tumor 		12 0 5 0.18 0 0
CUI: C0332886
Disease: Coarctation
Coarctation 		8 0 4 0.16 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		83 0 14 0.16 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 0 4 0.15 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 0 4 0.15 0 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy 		10 0 4 0.15 0 0
CUI: C0741276
Disease: ATRIAL ENLARGEMENT
ATRIAL ENLARGEMENT 		11 0 4 0.14 0 0
CUI: C1865926
Disease: Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)
Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) 		4 0 3 0.14 0 0
CUI: C2678367
Disease: Renal Tubular Dysgenesis With Choanal Atresia And Athelia
Renal Tubular Dysgenesis With Choanal Atresia And Athelia 		4 0 3 0.14 0 0
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		83 355 12 0.13 8 2.2E-02
CUI: C1854181
Disease: FIBROMATOSIS, GINGIVAL, 2
FIBROMATOSIS, GINGIVAL, 2 		6 0 3 0.12 0 0
CUI: C4021885
Disease: Atrial cardiomyopathy
Atrial cardiomyopathy 		7 0 3 0.12 0 0
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		74 0 10 0.12 0 0
CUI: C1839832
Disease: Noncompaction cardiomyopathy
Noncompaction cardiomyopathy 		17 0 4 0.12 0 0
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		8 0 3 0.12 0 0
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		8 0 3 0.12 0 0
CUI: C0266619
Disease: Potter's facies
Potter's facies 		9 0 3 0.11 0 0
CUI: C1333324
Disease: Barretts esophagus with dysplasia
Barretts esophagus with dysplasia 		9 0 3 0.11 0 0
CUI: C4509223
Disease: Heart failure with reduced ejection fraction [HFrEF]
Heart failure with reduced ejection fraction [HFrEF] 		9 0 3 0.11 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 5 0.11 0 0