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: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 8 0.14 0 0
CUI: C0340429
Disease: Familial restrictive cardiomyopathy (disorder)
Familial restrictive cardiomyopathy (disorder) 		3 0 2 0.14 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 3 0.14 0 0
CUI: C1864449
Disease: Limited neck flexion
Limited neck flexion 		3 0 2 0.14 0 0
CUI: C1864716
Disease: Intrinsic hand muscle atrophy
Intrinsic hand muscle atrophy 		11 0 3 0.14 0 0
CUI: C2931268
Disease: Scapuloperoneal myopathy
Scapuloperoneal myopathy 		3 0 2 0.14 0 0
CUI: C4024603
Disease: Atrophy of quadriceps femoris muscle
Atrophy of quadriceps femoris muscle 		3 0 2 0.14 0 0
CUI: C4531255
Disease: Internally nucleated skeletal muscle fibers
Internally nucleated skeletal muscle fibers 		3 0 2 0.14 0 0
CUI: C4552004
Disease: Distal Myopathy 1
Distal Myopathy 1 		3 0 2 0.14 0 0
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		61 0 9 0.14 0 0
CUI: C1842162
Disease: Scapuloperoneal amyotrophy
Scapuloperoneal amyotrophy 		4 0 2 0.13 0 0
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		30 0 5 0.13 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 0 6 0.13 0 0
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		22 0 4 0.13 0 0
CUI: C1836609
Disease: Progressive distal muscle weakness
Progressive distal muscle weakness 		14 0 3 0.12 0 0
CUI: C1837262
Disease: Increased muscle lipid content
Increased muscle lipid content 		14 0 3 0.12 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 3 0.12 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 9 0.12 0 0
CUI: C0577655
Disease: Quadriceps weakness
Quadriceps weakness 		15 0 3 0.12 0 0
CUI: C1832931
Disease: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 		6 0 2 0.12 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 2 0.12 0 0
CUI: C1866021
Disease: Increased connective tissue
Increased connective tissue 		16 0 3 0.12 0 0
CUI: C3645536
Disease: Autosomal Recessive Centronuclear Myopathy
Autosomal Recessive Centronuclear Myopathy 		16 0 3 0.12 0 0
CUI: C0751657
Disease: Nemaline Myopathy, Autosomal Recessive
Nemaline Myopathy, Autosomal Recessive 		7 0 2 0.11 0 0
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 0 5 0.11 0 0