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: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness
70 0 12 0.15 0 0
Partial Paralysis (Paresis) Vocal Cords
10 0 4 0.15 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy
59 0 10 0.14 0 0
Congenital hypomyelinating neuropathy
11 0 4 0.14 0 0
CUI: C0596992
Disease: myelinopathy
myelinopathy
3 0 3 0.14 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 0 17 0.14 0 0
CUI: C0040435
Disease: Tooth Diseases
Tooth Diseases
4 0 3 0.14 0 0
CUI: C1698196
Disease: Muscle Weakness Upper Limb
Muscle Weakness Upper Limb
29 0 6 0.14 0 0
CUI: C1836451
Disease: Distal lower limb amyotrophy
Distal lower limb amyotrophy
29 0 6 0.14 0 0
CUI: C1843168
Disease: Myelin outfoldings
Myelin outfoldings
4 0 3 0.14 0 0
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy
4 0 3 0.14 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy
106 0 15 0.13 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies
104 0 14 0.13 0 0
Hereditary, Type VII, Motor and Sensory Neuropathy
6 0 3 0.12 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb
42 0 7 0.12 0 0
CUI: C4024927
Disease: Peripheral hypomyelination
Peripheral hypomyelination
7 0 3 0.12 0 0
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder)
176 0 21 0.12 0 0
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration
17 0 4 0.12 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy
95 0 12 0.12 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes
28 0 5 0.11 0 0
CUI: C0270933
Disease: Inflammatory neuropathy
Inflammatory neuropathy
19 0 4 0.11 0 0
CUI: C1836450
Disease: Distal lower limb muscle weakness
Distal lower limb muscle weakness
49 0 7 0.11 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy
10 0 3 0.11 0 0
Charcot-Marie-Tooth disease, X-linked, 1
10 0 3 0.11 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy
10 0 3 0.11 0 0