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: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 19 0.20 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 0 29 0.18 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 11 20 0.16 1 4.2E-02
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 18 0.15 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 22 0.14 0 0
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity 		58 5 18 0.13 1 5.6E-02
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		208 136 34 0.13 2 1.4E-02
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 22 0.12 0 0
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 15 0.12 0 0
CUI: C0268630
Disease: Hyper-beta-alaninemia
Hyper-beta-alaninemia 		33 0 14 0.12 0 0
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		156 32 27 0.12 1 2.2E-02
CUI: C1842820
Disease: Cardiac conduction abnormality
Cardiac conduction abnormality 		18 0 12 0.12 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 13 0.12 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 21 0.12 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 12 0.12 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 12 0.12 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 12 0.12 0 0
CUI: C2931092
Disease: Maternally Inherited Leigh Syndrome
Maternally Inherited Leigh Syndrome 		12 0 11 0.11 0 0
CUI: C4021795
Disease: Abnormality of Krebs cycle metabolism
Abnormality of Krebs cycle metabolism 		12 0 11 0.11 0 0
CUI: C4022013
Disease: Multiple glomerular cysts
Multiple glomerular cysts 		12 0 11 0.11 0 0
CUI: C4025585
Disease: Lacticaciduria
Lacticaciduria 		12 0 11 0.11 0 0
CUI: C1856507
Disease: Bulbar signs
Bulbar signs 		33 0 13 0.11 0 0
CUI: C1839532
Disease: Low plasma citrulline
Low plasma citrulline 		14 0 11 0.11 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 41 0.11 0 0
CUI: C4531122
Disease: Abnormal speech prosody
Abnormal speech prosody 		15 0 11 0.11 0 0