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 29 0.28 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder)
26 0 16 0.28 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy
59 0 23 0.27 0 0
Hereditary Motor and Sensory Neuropathies
53 11 21 0.26 1 6.5E-03
Decreased number of peripheral myelinated nerve fibers
28 0 15 0.25 0 0
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy
64 20 22 0.24 2 1.2E-02
Hereditary Motor and Sensory Neuropathy Type I
19 84 13 0.24 1 4.4E-03
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness
70 4 22 0.23 1 6.8E-03
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
21 0 12 0.21 0 0
Hereditary motor and sensory neuropathy, types I-IV
21 0 12 0.21 0 0
Peroneal muscular atrophy (axonal type) (hypertrophic type)
21 0 12 0.21 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies
104 0 26 0.21 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe
46 0 15 0.19 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot
51 0 15 0.18 0 0
Decreased motor nerve conduction velocity
41 0 13 0.17 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 16 24 0.17 2 1.3E-02
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy
14 0 9 0.17 0 0
Charcot-Marie-Tooth Disease, Type Ia (disorder)
42 0 13 0.17 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
208 136 35 0.16 9 3.3E-02
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy
106 7 21 0.16 1 6.7E-03
CUI: C1836450
Disease: Distal lower limb muscle weakness
Distal lower limb muscle weakness
49 0 13 0.15 0 0
Charcot-Marie-Tooth Disease, Type Ib
12 51 8 0.15 1 5.2E-03
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
12 16 8 0.15 4 2.6E-02
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17
12 3 8 0.15 2 1.4E-02
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation
28 0 10 0.15 0 0