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: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
21 0 21 0.40 0 0
Hereditary motor and sensory neuropathy, types I-IV
21 0 21 0.40 0 0
Peroneal muscular atrophy (axonal type) (hypertrophic type)
21 0 21 0.40 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder)
26 0 22 0.39 0 0
Decreased motor nerve conduction velocity
41 0 22 0.31 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation
28 0 17 0.27 0 0
Hereditary Motor and Sensory-Neuropathy Type II
48 144 21 0.26 1 6.5E-03
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 28 0.25 0 0
Decreased number of peripheral myelinated nerve fibers
28 0 15 0.23 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies
104 0 27 0.21 0 0
Hereditary Motor and Sensory Neuropathy Type I
19 84 12 0.20 3 3.3E-02
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness
70 0 20 0.19 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe
46 0 16 0.19 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 0 27 0.19 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot
51 0 15 0.17 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
208 136 37 0.17 3 2.1E-02
Charcot-Marie-Tooth Disease, Type Ia (disorder)
42 0 13 0.16 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy
95 14 20 0.16 1 4.2E-02
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy
14 0 9 0.16 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4
14 77 9 0.16 2 2.3E-02
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy
59 0 15 0.15 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy
106 0 21 0.15 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration
8 0 8 0.15 0 0
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder)
176 0 28 0.14 0 0
Hereditary liability to pressure palsies
23 0 9 0.13 0 0