Source: ALL
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: C0393808
Disease: Charcot-Marie-Tooth disease, X-linked, 1
Charcot-Marie-Tooth disease, X-linked, 1 		10 0 4 8.3E-02 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 4 8.3E-02 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 7 8.1E-02 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy 		59 0 7 7.4E-02 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 0 11 7.4E-02 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 10 7.2E-02 0 0
CUI: C0270933
Disease: Inflammatory neuropathy
Inflammatory neuropathy 		19 0 4 7.0E-02 0 0
CUI: C0728829
Disease: Congenital pes cavus
Congenital pes cavus 		19 0 4 7.0E-02 0 0
CUI: C1843168
Disease: Myelin outfoldings
Myelin outfoldings 		4 0 3 7.0E-02 0 0
CUI: C0393819
Disease: Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating 		82 0 8 6.9E-02 0 0
CUI: C0027743
Disease: Nerve compression syndrome
Nerve compression syndrome 		5 0 3 6.8E-02 0 0
CUI: C1510429
Disease: Entrapment Neuropathies
Entrapment Neuropathies 		5 0 3 6.8E-02 0 0
CUI: C0043020
Disease: Wallerian Degeneration
Wallerian Degeneration 		21 0 4 6.8E-02 0 0
CUI: C0035022
Disease: Tick-borne relapsing fever
Tick-borne relapsing fever 		6 0 3 6.7E-02 0 0
CUI: C1832776
Disease: Hypertrophic nerve changes
Hypertrophic nerve changes 		6 0 3 6.7E-02 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		7 0 3 6.5E-02 0 0
CUI: C0154742
Disease: Other lesions of median nerve
Other lesions of median nerve 		8 0 3 6.4E-02 0 0
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		9 0 3 6.2E-02 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 3 6.2E-02 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 3 6.1E-02 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 3 6.1E-02 0 0
CUI: C1836451
Disease: Distal lower limb amyotrophy
Distal lower limb amyotrophy 		29 0 4 6.0E-02 0 0
CUI: C0221777
Disease: Nontoxic goiter
Nontoxic goiter 		13 0 3 5.8E-02 0 0
CUI: C0432185
Disease: Aplasia of muscle
Aplasia of muscle 		13 0 3 5.8E-02 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 0 3 5.7E-02 0 0