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: C1836003
Disease: Facial diplegia
Facial diplegia 		42 0 13 0.14 0 0
CUI: C0752282
Disease: Congenital Structural Myopathy
Congenital Structural Myopathy 		18 0 10 0.14 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 13 0.14 0 0
CUI: C0024003
Disease: Lordosis
Lordosis 		160 0 27 0.14 0 0
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		61 0 15 0.14 0 0
CUI: C0410203
Disease: X-linked centronuclear myopathy
X-linked centronuclear myopathy 		29 0 11 0.14 0 0
CUI: C3661489
Disease: Autosomal Dominant Myotubular Myopathy
Autosomal Dominant Myotubular Myopathy 		13 0 9 0.13 0 0
CUI: C4551952
Disease: Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 1 		13 0 9 0.13 0 0
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		30 0 11 0.13 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 9 0.13 0 0
CUI: C1834558
Disease: Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Centronuclear, Autosomal Dominant 		16 0 9 0.13 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 13 0.12 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		126 0 21 0.12 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 10 0.12 0 0
CUI: C1850674
Disease: MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder)
MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder) 		11 0 8 0.12 0 0
CUI: C0332878
Disease: Congenital contracture
Congenital contracture 		31 0 10 0.12 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		182 0 26 0.12 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 28 0.12 0 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 19 0.12 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 12 0.12 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 14 0.12 0 0
CUI: C0234860
Disease: Weak cry
Weak cry 		42 0 11 0.12 0 0
CUI: C4022583
Disease: Fatiguable weakness of proximal limb muscles
Fatiguable weakness of proximal limb muscles 		14 0 8 0.12 0 0
CUI: C4022591
Disease: Fatigable weakness of bulbar muscles
Fatigable weakness of bulbar muscles 		14 0 8 0.12 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 24 0.12 0 0