Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Hereditary motor and sensory neuropathy, types I-IV
21 0 21 1.00 0 0
Peroneal muscular atrophy (axonal type) (hypertrophic type)
21 0 21 1.00 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder)
26 0 21 0.81 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation
28 0 15 0.44 0 0
Hereditary Motor and Sensory Neuropathies
53 0 21 0.40 0 0
Decreased motor nerve conduction velocity
41 0 17 0.38 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration
8 0 7 0.32 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4
14 0 8 0.30 0 0
Decreased number of peripheral myelinated nerve fibers
28 0 11 0.29 0 0
Hereditary Motor and Sensory Neuropathy Type I
19 0 8 0.25 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw
9 0 6 0.25 0 0
Charcot-Marie-Tooth Disease, Type Ib
12 0 6 0.22 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 19 0.22 0 0
CUI: C0728829
Disease: Congenital pes cavus
Congenital pes cavus
19 0 7 0.21 0 0
Hereditary Motor and Sensory-Neuropathy Type II
48 0 12 0.21 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy
14 0 6 0.21 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe
46 0 11 0.20 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot
51 0 11 0.18 0 0
CUI: C1832776
Disease: Hypertrophic nerve changes
Hypertrophic nerve changes
6 0 4 0.17 0 0
Charcot-Marie-Tooth Disease, Type Ia (disorder)
42 0 9 0.17 0 0
Segmental peripheral demyelination/remyelination
21 0 6 0.17 0 0
Charcot-Marie-Tooth disease, Type 2A
7 0 4 0.17 0 0
Hereditary liability to pressure palsies
23 0 6 0.16 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy
9 0 4 0.15 0 0
CUI: C4025830
Disease: Peripheral axonal degeneration
Peripheral axonal degeneration
9 0 4 0.15 0 0