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: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 5 10 0.36 5 9.8E-02
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		19 84 8 0.35 28 0.26
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 6 0.22 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 6 0.22 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 6 0.22 0 0
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 8 0.17 0 0
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized 		2 0 2 0.17 0 0
CUI: C1861675
Disease: Cold-induced muscle cramps
Cold-induced muscle cramps 		2 0 2 0.17 0 0
CUI: C4016264
Disease: DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT 		2 6 2 0.17 2 3.6E-02
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 3 0.17 0 0
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 144 8 0.15 1 5.2E-03
CUI: C1858278
Disease: Charcot-Marie-Tooth disease, Type 4B2
Charcot-Marie-Tooth disease, Type 4B2 		3 0 2 0.15 0 0
CUI: C4025132
Disease: Shortening of all distal phalanges of the toes
Shortening of all distal phalanges of the toes 		3 0 2 0.15 0 0
CUI: C1843168
Disease: Myelin outfoldings
Myelin outfoldings 		4 0 2 0.14 0 0
CUI: C0027743
Disease: Nerve compression syndrome
Nerve compression syndrome 		5 0 2 0.13 0 0
CUI: C1510429
Disease: Entrapment Neuropathies
Entrapment Neuropathies 		5 0 2 0.13 0 0
CUI: C1832399
Disease: Charcot-Marie-Tooth disease, Type 4B1
Charcot-Marie-Tooth disease, Type 4B1 		5 0 2 0.13 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 0 3 0.13 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 6 0.13 0 0
CUI: C0019816
Disease: Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy 		6 0 2 0.12 0 0
CUI: C0579144
Disease: Cavovarus deformity of foot
Cavovarus deformity of foot 		6 0 2 0.12 0 0
CUI: C1832776
Disease: Hypertrophic nerve changes
Hypertrophic nerve changes 		6 0 2 0.12 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 11 7 0.12 3 5.1E-02
CUI: C0034933
Disease: Reflex, Abnormal
Reflex, Abnormal 		7 0 2 0.12 0 0
CUI: C0521532
Disease: Diaphragmatic paresis
Diaphragmatic paresis 		8 0 2 0.11 0 0