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: C0019816
Disease: Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy 		6 0 4 0.50 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 5 0.50 0 0
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized 		2 0 2 0.33 0 0
CUI: C1861675
Disease: Cold-induced muscle cramps
Cold-induced muscle cramps 		2 0 2 0.33 0 0
CUI: C4016264
Disease: DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT 		2 0 2 0.33 0 0
CUI: C4721436
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE
NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE 		2 0 2 0.33 0 0
CUI: C0596992
Disease: myelinopathy
myelinopathy 		3 0 2 0.29 0 0
CUI: C1866637
Disease: Basal lamina onion bulb formation
Basal lamina onion bulb formation 		3 0 2 0.29 0 0
CUI: C1843168
Disease: Myelin outfoldings
Myelin outfoldings 		4 0 2 0.25 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 5 0.23 0 0
CUI: C0027743
Disease: Nerve compression syndrome
Nerve compression syndrome 		5 0 2 0.22 0 0
CUI: C1510429
Disease: Entrapment Neuropathies
Entrapment Neuropathies 		5 0 2 0.22 0 0
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		11 0 3 0.21 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 6 0.21 0 0
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		19 0 4 0.19 0 0
CUI: C0270913
Disease: Charcot-Marie-Tooth disease, Type 1C
Charcot-Marie-Tooth disease, Type 1C 		7 0 2 0.18 0 0
CUI: C4024927
Disease: Peripheral hypomyelination
Peripheral hypomyelination 		7 0 2 0.18 0 0
CUI: C2932678
Disease: Inherited Peripheral Neuropathy
Inherited Peripheral Neuropathy 		14 0 3 0.18 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 0 3 0.18 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 4 0.17 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 4 0.17 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 4 0.17 0 0
CUI: C1858285
Disease: Decreased number of peripheral myelinated nerve fibers
Decreased number of peripheral myelinated nerve fibers 		28 0 5 0.17 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil 		1 0 1 0.17 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 0.17 0 0