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: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 5 30 0.20 1 4.0E-02
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		95 0 29 0.18 0 0
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		156 32 35 0.16 1 1.9E-02
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		94 0 26 0.16 0 0
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity 		58 0 20 0.15 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 15 0.15 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 40 0.15 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 17 34 0.15 3 8.6E-02
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 25 0.14 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy 		59 0 19 0.14 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 50 0.14 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 16 34 0.13 2 5.7E-02
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 16 24 0.13 2 5.7E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 144 16 0.13 1 6.1E-03
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers 		59 0 17 0.13 0 0
CUI: C0268630
Disease: Hyper-beta-alaninemia
Hyper-beta-alaninemia 		33 0 14 0.12 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 21 0.12 0 0
CUI: C2931092
Disease: Maternally Inherited Leigh Syndrome
Maternally Inherited Leigh Syndrome 		12 0 11 0.12 0 0
CUI: C4021795
Disease: Abnormality of Krebs cycle metabolism
Abnormality of Krebs cycle metabolism 		12 0 11 0.12 0 0
CUI: C4022013
Disease: Multiple glomerular cysts
Multiple glomerular cysts 		12 0 11 0.12 0 0
CUI: C4025585
Disease: Lacticaciduria
Lacticaciduria 		12 0 11 0.12 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 4 17 0.12 1 4.2E-02
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		61 0 16 0.12 0 0
CUI: C1839532
Disease: Low plasma citrulline
Low plasma citrulline 		14 0 11 0.11 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 0 15 0.11 0 0