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: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		83 355 64 0.11 203 0.26
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
Hypertrophic obstructive cardiomyopathy 		233 90 230 0.41 88 0.14
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 163 9 1.6E-02 78 0.11
CUI: C1861862
Disease: Familial Hypertrophic Cardiomyopathy Type 4
Familial Hypertrophic Cardiomyopathy Type 4 		3 145 2 3.6E-03 60 8.3E-02
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		925 294 256 0.21 57 6.5E-02
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		773 243 181 0.16 24 2.8E-02
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
Cardiomyopathy, Familial Hypertrophic, 2 		1 30 1 1.8E-03 16 2.5E-02
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
LEFT VENTRICULAR NONCOMPACTION 10 		1 20 1 1.8E-03 14 2.2E-02
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
CARDIOMYOPATHY, DILATED, 1D (disorder) 		1 24 1 1.8E-03 13 2.0E-02
CUI: C4552004
Disease: Distal Myopathy 1
Distal Myopathy 1 		3 36 2 3.6E-03 13 2.0E-02
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 53 7 1.2E-02 13 1.9E-02
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		403 67 125 0.15 13 1.9E-02
CUI: C1860752
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 		1 15 1 1.8E-03 12 1.9E-02
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder) 		1 21 1 1.8E-03 12 1.9E-02
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		512 509 165 0.18 20 1.8E-02
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		7 15 5 8.9E-03 11 1.7E-02
CUI: C0751337
Disease: X-Linked Emery-Dreifuss Muscular Dystrophy
X-Linked Emery-Dreifuss Muscular Dystrophy 		20 33 9 1.6E-02 11 1.7E-02
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 30 17 2.9E-02 10 1.5E-02
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		33 49 10 1.7E-02 10 1.5E-02
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 11 1 1.8E-03 9 1.4E-02
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 24 16 2.8E-02 9 1.4E-02
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		47 27 27 4.7E-02 8 1.2E-02
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		1760 165 282 0.14 9 1.1E-02
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		23 83 12 2.1E-02 8 1.1E-02
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		85 187 30 4.9E-02 9 1.1E-02