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: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 8 0.30 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 8 0.30 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 8 0.30 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 0 8 0.25 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 8 0.24 0 0
CUI: C1858278
Disease: Charcot-Marie-Tooth disease, Type 4B2
Charcot-Marie-Tooth disease, Type 4B2 		3 0 3 0.21 0 0
CUI: C1866637
Disease: Basal lamina onion bulb formation
Basal lamina onion bulb formation 		3 0 3 0.21 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 4 0.21 0 0
CUI: C1832399
Disease: Charcot-Marie-Tooth disease, Type 4B1
Charcot-Marie-Tooth disease, Type 4B1 		5 5 3 0.19 2 2.5E-02
CUI: C1832776
Disease: Hypertrophic nerve changes
Hypertrophic nerve changes 		6 0 3 0.18 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 8 0.17 0 0
CUI: C4024927
Disease: Peripheral hypomyelination
Peripheral hypomyelination 		7 0 3 0.17 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 11 9 0.16 2 2.3E-02
CUI: C1854510
Disease: Abnormality of the cranial nerves
Abnormality of the cranial nerves 		17 0 4 0.15 0 0
CUI: C1858285
Disease: Decreased number of peripheral myelinated nerve fibers
Decreased number of peripheral myelinated nerve fibers 		28 0 5 0.14 0 0
CUI: C0270912
Disease: Charcot-Marie-Tooth Disease, Type Ib
Charcot-Marie-Tooth Disease, Type Ib 		12 0 3 0.13 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 4 0.13 0 0
CUI: C0040435
Disease: Tooth Diseases
Tooth Diseases 		4 0 2 0.12 0 0
CUI: C1859606
Disease: Decreased number of large peripheral myelinated nerve fibers
Decreased number of large peripheral myelinated nerve fibers 		14 0 3 0.12 0 0
CUI: C3711383
Disease: Early-Onset Glaucoma
Early-Onset Glaucoma 		15 0 3 0.12 0 0
CUI: C0019816
Disease: Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy 		6 0 2 0.11 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 10 0.11 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		95 14 10 0.10 2 2.2E-02
CUI: C4025830
Disease: Peripheral axonal degeneration
Peripheral axonal degeneration 		9 0 2 9.5E-02 0 0
CUI: C0343239
Disease: Benign congenital hypotonia
Benign congenital hypotonia 		11 0 2 8.7E-02 0 0