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: C1854494
Disease: Slow progression
Slow progression 		165 0 17 8.5E-02 0 0
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		26 0 6 8.2E-02 0 0
CUI: C0878575
Disease: Peripheral demyelination
Peripheral demyelination 		27 0 6 8.1E-02 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes 		28 0 6 8.0E-02 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 27 8.0E-02 0 0
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		351 0 29 7.7E-02 0 0
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		156 0 15 7.7E-02 0 0
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration 		17 0 5 7.7E-02 0 0
CUI: C0271683
Disease: Polyneuropathy, Motor
Polyneuropathy, Motor 		32 0 6 7.6E-02 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs 		18 0 5 7.6E-02 0 0
CUI: C0280325
Disease: Glottic Squamous Cell Carcinoma
Glottic Squamous Cell Carcinoma 		4 0 4 7.5E-02 0 0
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy 		4 0 4 7.5E-02 0 0
CUI: C0270933
Disease: Inflammatory neuropathy
Inflammatory neuropathy 		19 0 5 7.5E-02 0 0
CUI: C0221373
Disease: Claw hand
Claw hand 		63 0 8 7.4E-02 0 0
CUI: C1853710
Disease: HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)
HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder) 		5 0 4 7.4E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 0 5 7.2E-02 0 0
CUI: C4024927
Disease: Peripheral hypomyelination
Peripheral hypomyelination 		7 0 4 7.1E-02 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy 		9 0 4 6.9E-02 0 0
CUI: C4025830
Disease: Peripheral axonal degeneration
Peripheral axonal degeneration 		9 0 4 6.9E-02 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 4 6.8E-02 0 0
CUI: C0393808
Disease: Charcot-Marie-Tooth disease, X-linked, 1
Charcot-Marie-Tooth disease, X-linked, 1 		10 0 4 6.8E-02 0 0
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity 		58 0 7 6.7E-02 0 0
CUI: C1833308
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V 		12 0 4 6.6E-02 0 0
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17 		12 0 4 6.6E-02 0 0
CUI: C0442874
Disease: Neuropathy
Neuropathy 		484 110 32 6.3E-02 3 2.5E-02