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: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
208 0 57 0.22 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 34 0.22 0 0
Hereditary Motor and Sensory Neuropathies
53 0 27 0.21 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy
106 0 36 0.21 0 0
Hereditary Motor and Sensory-Neuropathy Type II
48 0 26 0.21 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 0 34 0.18 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus
213 0 48 0.18 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy
59 0 24 0.17 0 0
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy
64 0 24 0.17 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot
51 0 20 0.15 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe
46 0 19 0.15 0 0
Decreased motor nerve conduction velocity
41 0 18 0.14 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder)
26 0 16 0.14 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness
70 0 20 0.13 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 35 0.13 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation
28 0 15 0.13 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
21 0 14 0.13 0 0
Hereditary motor and sensory neuropathy, types I-IV
21 0 14 0.13 0 0
Peroneal muscular atrophy (axonal type) (hypertrophic type)
21 0 14 0.13 0 0
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy
94 0 22 0.12 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy
95 0 22 0.12 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy
93 0 21 0.12 0 0
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
116 0 23 0.12 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 27 0.11 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 41 0.11 0 0