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: C0751336
Disease: Distal Muscular Dystrophies
Distal Muscular Dystrophies 		31 18 18 0.24 2 5.0E-02
CUI: C1836057
Disease: Muscle fiber splitting
Muscle fiber splitting 		13 0 9 0.14 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 15 0.14 0 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy 		10 0 8 0.13 0 0
CUI: C0238190
Disease: Inclusion Body Myositis (disorder)
Inclusion Body Myositis (disorder) 		87 0 16 0.12 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		47 0 11 0.11 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		18 0 8 0.11 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		28 0 9 0.11 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 13 0.11 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 7 11 0.11 2 6.9E-02
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 11 0.10 0 0
CUI: C0039496
Disease: Temporomandibular Joint Dysfunction Syndrome
Temporomandibular Joint Dysfunction Syndrome 		24 0 8 0.10 0 0
CUI: C0333440
Disease: Hyaline body
Hyaline body 		14 0 7 0.10 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 4 10 9.9E-02 1 3.7E-02
CUI: C1853932
Disease: Rimmed vacuoles on biopsy
Rimmed vacuoles on biopsy 		28 2 8 9.9E-02 1 4.0E-02
CUI: C0751713
Disease: Inclusion Body Myopathy, Sporadic
Inclusion Body Myopathy, Sporadic 		84 0 13 9.8E-02 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 24 7 9.3E-02 1 2.1E-02
CUI: C0410180
Disease: Eichsfeld type congenital muscular dystrophy
Eichsfeld type congenital muscular dystrophy 		10 0 6 9.2E-02 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		83 0 12 9.1E-02 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 8 14 8.7E-02 1 3.2E-02
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 0 23 8.6E-02 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 14 8.6E-02 0 0
CUI: C0521858
Disease: Decreased drug resistance
Decreased drug resistance 		15 0 6 8.6E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 30 8 8.5E-02 1 1.9E-02
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 6 9 8.3E-02 1 3.4E-02