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: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
116 15 30 0.10 2 1.3E-02
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
21 0 21 0.10 0 0
Hereditary motor and sensory neuropathy, types I-IV
21 0 21 0.10 0 0
Peroneal muscular atrophy (axonal type) (hypertrophic type)
21 0 21 0.10 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe
46 0 22 9.5E-02 0 0
Hereditary Motor and Sensory Neuropathy Type I
19 84 19 9.1E-02 20 1.0E-01
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases
171 50 31 8.9E-02 6 3.3E-02
Decreased number of peripheral myelinated nerve fibers
28 0 19 8.8E-02 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease
186 52 31 8.5E-02 1 5.3E-03
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder)
176 45 30 8.5E-02 10 5.8E-02
CUI: C0026847
Disease: Spinal Muscular Atrophy
Spinal Muscular Atrophy
320 0 40 8.2E-02 0 0
CUI: C0030552
Disease: Paresis
Paresis
216 49 32 8.2E-02 1 5.4E-03
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
536 87 54 7.8E-02 1 4.5E-03
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy
138 0 25 7.8E-02 0 0
CUI: C1836450
Disease: Distal lower limb muscle weakness
Distal lower limb muscle weakness
49 0 18 7.5E-02 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 0 30 7.5E-02 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy
14 0 14 6.7E-02 0 0
CUI: C0037763
Disease: Spasm
Spasm
172 0 23 6.4E-02 0 0
CUI: C1836296
Disease: Muscle Weakness Lower Limb
Muscle Weakness Lower Limb
74 0 17 6.4E-02 0 0
CUI: C0027809
Disease: Neurilemmoma
Neurilemmoma
193 0 24 6.4E-02 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes
28 0 14 6.3E-02 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4
14 77 13 6.2E-02 8 3.9E-02
CUI: C0016506
Disease: Foot Deformities
Foot Deformities
66 0 16 6.2E-02 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy
306 0 29 6.0E-02 0 0
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity
58 0 15 6.0E-02 0 0