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: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
21 0 21 0.81 0 0
Hereditary motor and sensory neuropathy, types I-IV
21 0 21 0.81 0 0
Peroneal muscular atrophy (axonal type) (hypertrophic type)
21 0 21 0.81 0 0
Hereditary Motor and Sensory Neuropathies
53 0 22 0.39 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation
28 0 15 0.38 0 0
Decreased motor nerve conduction velocity
41 0 18 0.37 0 0
Hereditary Motor and Sensory Neuropathy Type I
19 84 12 0.36 4 4.7E-02
Charcot-Marie-Tooth Disease, Type Ib
12 51 10 0.36 5 9.8E-02
Hereditary Motor and Sensory-Neuropathy Type II
48 0 16 0.28 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration
8 0 7 0.26 0 0
Decreased number of peripheral myelinated nerve fibers
28 0 11 0.26 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4
14 0 8 0.25 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 22 0.24 0 0
Charcot-Marie-Tooth Disease, Type Ia (disorder)
42 0 13 0.24 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw
9 0 6 0.21 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe
46 0 12 0.20 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot
51 0 12 0.18 0 0
CUI: C0728829
Disease: Congenital pes cavus
Congenital pes cavus
19 0 7 0.18 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy
14 0 6 0.18 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness
70 0 14 0.17 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy
10 0 5 0.16 0 0
Partial Paralysis (Paresis) Vocal Cords
10 0 5 0.16 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy
59 0 11 0.15 0 0
Segmental peripheral demyelination/remyelination
21 0 6 0.15 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 0 18 0.14 0 0