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: C0577655
Disease: Quadriceps weakness
Quadriceps weakness 		15 1 5 0.10 1 0.33
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 7 24 0.37 2 0.25
CUI: C0427064
Disease: Pelvic girdle weakness
Pelvic girdle weakness 		16 2 8 0.17 1 0.25
CUI: C1842062
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F 		1 3 1 2.6E-02 1 0.20
CUI: C1860121
Disease: Decreased testosterone in males
Decreased testosterone in males 		2 3 1 2.6E-02 1 0.20
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 4 9 0.13 1 0.17
CUI: C4310645
Disease: MYOPATHY, MYOFIBRILLAR, 8
MYOPATHY, MYOFIBRILLAR, 8 		1 5 1 2.6E-02 1 0.14
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 6 10 0.12 1 0.12
CUI: C1858091
Disease: Long fingers
Long fingers 		32 6 5 7.7E-02 1 0.12
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 6 1 1.8E-02 1 0.12
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 16 15 0.11 2 0.12
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 8 21 0.16 1 1.0E-01
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 8 17 0.23 1 1.0E-01
CUI: C0037763
Disease: Spasm
Spasm 		172 9 11 5.5E-02 1 9.1E-02
CUI: C0018808
Disease: Heart murmur
Heart murmur 		31 10 2 3.0E-02 1 8.3E-02
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 11 18 0.14 1 7.7E-02
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 12 14 4.2E-02 1 7.1E-02
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 15 6 7.9E-02 1 5.9E-02
CUI: C0231528
Disease: Myalgia
Myalgia 		226 22 9 3.5E-02 1 4.2E-02
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		61 24 7 7.6E-02 1 3.8E-02
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 30 27 0.11 1 3.1E-02
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		280 67 14 4.6E-02 2 2.9E-02
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 43 23 9.5E-02 1 2.2E-02
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		30 46 4 6.2E-02 1 2.1E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		389 50 11 2.6E-02 1 1.9E-02