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: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy 		19 0 8 0.12 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 8 18 0.12 1 7.7E-02
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 3 10 0.12 1 0.12
CUI: C3808250
Disease: Reduced forced vital capacity
Reduced forced vital capacity 		10 0 7 0.12 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 11 0.12 0 0
CUI: C1850573
Disease: Slender build
Slender build 		31 0 9 0.12 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 12 0.12 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 7 0.11 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology 		13 0 7 0.11 0 0
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		33 0 9 0.11 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 12 0.11 0 0
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 15 10 0.11 2 0.11
CUI: C1837098
Disease: Easy fatigability
Easy fatigability 		74 0 13 0.11 0 0
CUI: C1843643
Disease: Nocturnal hypoventilation
Nocturnal hypoventilation 		14 0 7 0.11 0 0
CUI: C0333751
Disease: Muscle fiber atrophy
Muscle fiber atrophy 		25 0 8 0.11 0 0
CUI: C0026884
Disease: Mutism
Mutism 		47 0 10 0.11 0 0
CUI: C0086439
Disease: Hypokinesia
Hypokinesia 		47 0 10 0.11 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 0 9 0.10 0 0
CUI: C1276035
Disease: Pena-Shokeir syndrome type I
Pena-Shokeir syndrome type I 		40 0 9 0.10 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 9 0.10 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb 		42 3 9 0.10 2 0.29
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 7 1.0E-01 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 7 9.7E-02 0 0
CUI: C1865412
Disease: Abnormal lower motor neuron morphology
Abnormal lower motor neuron morphology 		23 0 7 9.7E-02 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 12 32 9.7E-02 1 5.9E-02