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: C0877009
Disease: Muscle fibrosis
Muscle fibrosis 		34 0 6 6.1E-02 0 0
CUI: C1834674
Disease: BETHLEM MYOPATHY 1
BETHLEM MYOPATHY 1 		17 0 5 6.1E-02 0 0
CUI: C1839666
Disease: Calf muscle pseudohypertrophy
Calf muscle pseudohypertrophy 		17 0 5 6.1E-02 0 0
CUI: C0026848
Disease: Myopathy
Myopathy 		634 166 40 6.0E-02 2 1.2E-02
CUI: C1869123
Disease: Limb-girdle muscular dystrophy type 2A
Limb-girdle muscular dystrophy type 2A 		18 0 5 6.0E-02 0 0
CUI: C0024003
Disease: Lordosis
Lordosis 		160 0 13 6.0E-02 0 0
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 0 7 6.0E-02 0 0
CUI: C0393642
Disease: Sepsis-Associated Encephalopathy
Sepsis-Associated Encephalopathy 		57 0 7 5.8E-02 0 0
CUI: C0920646
Disease: Ischemia of kidney
Ischemia of kidney 		131 0 11 5.8E-02 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 6 5.7E-02 0 0
CUI: C0019151
Disease: Hepatic Encephalopathy
Hepatic Encephalopathy 		100 0 9 5.6E-02 0 0
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities 		83 20 8 5.5E-02 1 4.5E-02
CUI: C1852502
Disease: CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT 		45 0 6 5.5E-02 0 0
CUI: C2827469
Disease: Coronary Microvascular Disease
Coronary Microvascular Disease 		45 0 6 5.5E-02 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		47 0 6 5.4E-02 0 0
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE 		67 0 7 5.4E-02 0 0
CUI: C2936332
Disease: Alpha-Sarcoglycanopathies
Alpha-Sarcoglycanopathies 		9 0 4 5.3E-02 0 0
CUI: C0410180
Disease: Eichsfeld type congenital muscular dystrophy
Eichsfeld type congenital muscular dystrophy 		10 0 4 5.3E-02 0 0
CUI: C0427144
Disease: Toe-walking gait
Toe-walking gait 		50 0 6 5.3E-02 0 0
CUI: C1843637
Disease: Neck flexor weakness
Neck flexor weakness 		30 0 5 5.3E-02 0 0
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		11 54 4 5.2E-02 1 1.8E-02
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 0 9 5.2E-02 0 0
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
Fuchs Endothelial Dystrophy 		94 0 8 5.1E-02 0 0
CUI: C1847766
Disease: Shoulder girdle muscle atrophy
Shoulder girdle muscle atrophy 		12 0 4 5.1E-02 0 0
CUI: C0270952
Disease: Muscular Dystrophy, Oculopharyngeal
Muscular Dystrophy, Oculopharyngeal 		33 0 5 5.1E-02 0 0