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: C1837262
Disease: Increased muscle lipid content
Increased muscle lipid content 		14 0 9 0.35 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset 		7 0 7 0.33 0 0
CUI: C4022591
Disease: Fatigable weakness of bulbar muscles
Fatigable weakness of bulbar muscles 		14 0 8 0.30 0 0
CUI: C4025729
Disease: Neuromuscular dysphagia
Neuromuscular dysphagia 		12 0 7 0.27 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 7 0.24 0 0
CUI: C4022583
Disease: Fatiguable weakness of proximal limb muscles
Fatiguable weakness of proximal limb muscles 		14 0 6 0.21 0 0
CUI: C3710589
Disease: Cap Myopathy
Cap Myopathy 		9 0 5 0.20 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 8 0.19 0 0
CUI: C4025571
Disease: Type 1 fibers relatively smaller than type 2 fibers
Type 1 fibers relatively smaller than type 2 fibers 		6 0 4 0.17 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 10 0.17 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 5 0.17 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 9 0.16 0 0
CUI: C4022585
Disease: Fatigable weakness of distal limb muscles
Fatigable weakness of distal limb muscles 		8 0 4 0.16 0 0
CUI: C4025008
Disease: Reduced systolic function
Reduced systolic function 		8 0 4 0.16 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		30 0 7 0.16 0 0
CUI: C1850573
Disease: Slender build
Slender build 		31 0 7 0.16 0 0
CUI: C0233844
Disease: Clumsiness
Clumsiness 		48 0 9 0.15 0 0
CUI: C1856507
Disease: Bulbar signs
Bulbar signs 		33 0 7 0.15 0 0
CUI: C3808250
Disease: Reduced forced vital capacity
Reduced forced vital capacity 		10 0 4 0.15 0 0
CUI: C1836003
Disease: Facial diplegia
Facial diplegia 		42 0 8 0.15 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance 		76 0 12 0.14 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		28 0 6 0.14 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		47 0 8 0.13 0 0
CUI: C3661489
Disease: Autosomal Dominant Myotubular Myopathy
Autosomal Dominant Myotubular Myopathy 		13 0 4 0.13 0 0
CUI: C4551952
Disease: Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 1 		13 0 4 0.13 0 0