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 0 57 0.24 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 57 0.22 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 16 50 0.18 1 6.6E-03
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 2 63 0.18 1 7.3E-03
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 11 37 0.17 3 2.1E-02
CUI: C0442874
Disease: Neuropathy
Neuropathy 		484 110 96 0.16 20 8.8E-02
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		351 81 77 0.16 5 2.4E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 144 35 0.16 9 3.3E-02
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy 		59 13 36 0.16 3 2.1E-02
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 55 0.16 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 4 35 0.14 1 7.2E-03
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 31 0.14 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 7 39 0.14 2 1.4E-02
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 32 0.14 0 0
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases 		549 69 93 0.14 6 3.0E-02
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		95 14 34 0.13 2 1.4E-02
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 5 26 0.12 3 2.2E-02
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy 		64 20 30 0.12 3 2.0E-02
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 56 0.12 0 0
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		156 32 38 0.12 2 1.2E-02
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 38 0.11 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 24 0.11 0 0
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 24 25 0.11 3 1.9E-02
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 21 30 0.11 3 1.9E-02
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		94 12 30 0.11 1 6.8E-03