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: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 43 180 0.26 4 2.0E-02
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		536 87 211 0.22 17 7.2E-02
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		925 294 253 0.19 10 2.2E-02
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		512 509 163 0.17 7 1.0E-02
CUI: C0030552
Disease: Paresis
Paresis 		216 49 115 0.16 12 5.9E-02
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		280 67 122 0.15 5 2.2E-02
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 12 125 0.15 1 5.6E-03
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		560 635 157 0.15 5 6.3E-03
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		130 0 97 0.15 0 0
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases 		171 50 102 0.15 1 4.7E-03
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		1760 165 262 0.12 4 1.2E-02
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		773 243 152 0.12 7 1.7E-02
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 0 151 0.12 0 0
CUI: C0231528
Disease: Myalgia
Myalgia 		226 22 91 0.12 3 1.6E-02
CUI: C0033377
Disease: Ptosis
Ptosis 		607 0 131 0.12 0 0
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		403 67 109 0.12 2 8.7E-03
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		595 57 128 0.12 1 4.5E-03
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 16 78 0.12 9 5.2E-02
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		375 170 104 0.11 1 3.0E-03
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 11 76 0.11 1 5.7E-03
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 135 151 0.11 4 1.3E-02
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		226 0 86 0.11 0 0
CUI: C1145670
Disease: Respiratory Failure
Respiratory Failure 		319 23 95 0.11 1 5.3E-03
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 94 0.11 0 0
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
Hypertrophic obstructive cardiomyopathy 		233 90 86 0.11 4 1.6E-02