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 79 0.18 8 7.8E-02
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		10 74 7 2.5E-02 7 5.2E-02
CUI: C0241237
Disease: Difficulty standing
Difficulty standing 		21 14 7 2.4E-02 6 8.0E-02
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 30 33 7.0E-02 6 6.6E-02
CUI: C0026848
Disease: Myopathy
Myopathy 		634 166 122 0.15 5 2.2E-02
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 8 31 0.10 5 7.1E-02
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		44 18 11 3.5E-02 5 6.2E-02
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		536 87 88 0.12 4 2.7E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 144 4 1.2E-02 4 1.9E-02
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle 		118 37 62 0.18 4 4.0E-02
CUI: C0751336
Disease: Distal Muscular Dystrophies
Distal Muscular Dystrophies 		31 18 20 6.9E-02 4 4.9E-02
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		773 243 63 6.4E-02 4 1.3E-02
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy 		15 4 10 3.5E-02 4 6.0E-02
CUI: C1850889
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B 		19 150 10 3.5E-02 4 1.9E-02
CUI: C1869123
Disease: Limb-girdle muscular dystrophy type 2A
Limb-girdle muscular dystrophy type 2A 		18 146 13 4.6E-02 4 1.9E-02
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		375 170 101 0.18 3 1.3E-02
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 8 38 0.11 3 4.2E-02
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 15 13 4.2E-02 3 3.8E-02
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 20 42 0.14 3 3.6E-02
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 6 17 5.3E-02 3 4.3E-02
CUI: C1836296
Disease: Muscle Weakness Lower Limb
Muscle Weakness Lower Limb 		74 15 9 2.6E-02 3 3.8E-02
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		61 24 18 5.6E-02 3 3.4E-02
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 16 45 0.13 3 3.7E-02
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		512 509 61 8.3E-02 2 3.5E-03
CUI: C0158113
Disease: Contracture of joint of hand
Contracture of joint of hand 		55 5 7 2.1E-02 2 2.9E-02