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: C1853171
Disease: Multiple prenatal fractures
Multiple prenatal fractures 		15 0 9 0.25 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 9 0.25 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset 		7 0 7 0.23 0 0
CUI: C4025729
Disease: Neuromuscular dysphagia
Neuromuscular dysphagia 		12 0 7 0.20 0 0
CUI: C1837262
Disease: Increased muscle lipid content
Increased muscle lipid content 		14 0 7 0.19 0 0
CUI: C4022583
Disease: Fatiguable weakness of proximal limb muscles
Fatiguable weakness of proximal limb muscles 		14 0 7 0.19 0 0
CUI: C4022591
Disease: Fatigable weakness of bulbar muscles
Fatigable weakness of bulbar muscles 		14 0 7 0.19 0 0
CUI: C1838114
Disease: Generalized limb muscle atrophy
Generalized limb muscle atrophy 		21 0 7 0.16 0 0
CUI: C4022585
Disease: Fatigable weakness of distal limb muscles
Fatigable weakness of distal limb muscles 		8 0 5 0.15 0 0
CUI: C1276035
Disease: Pena-Shokeir syndrome type I
Pena-Shokeir syndrome type I 		40 0 9 0.15 0 0
CUI: C2732374
Disease: Edema of dorsum of hand
Edema of dorsum of hand 		9 0 5 0.15 0 0
CUI: C3710589
Disease: Cap Myopathy
Cap Myopathy 		9 0 5 0.15 0 0
CUI: C1836003
Disease: Facial diplegia
Facial diplegia 		42 0 9 0.14 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 9 0.14 0 0
CUI: C1848873
Disease: Abnormality of the diaphragm
Abnormality of the diaphragm 		12 0 5 0.14 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 7 0.13 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		47 0 9 0.13 0 0
CUI: C1850573
Disease: Slender build
Slender build 		31 0 7 0.13 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 5 0.13 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 9 0.13 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb 		42 0 8 0.12 0 0
CUI: C1856507
Disease: Bulbar signs
Bulbar signs 		33 0 7 0.12 0 0
CUI: C1866021
Disease: Increased connective tissue
Increased connective tissue 		16 0 5 0.12 0 0
CUI: C0751657
Disease: Nemaline Myopathy, Autosomal Recessive
Nemaline Myopathy, Autosomal Recessive 		7 0 4 0.12 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		28 0 6 0.12 0 0