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: C1858280
Disease: Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma
Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma 		1 0 1 1.00 0 0
CUI: C1858278
Disease: Charcot-Marie-Tooth disease, Type 4B2
Charcot-Marie-Tooth disease, Type 4B2 		3 0 1 0.33 0 0
CUI: C1832399
Disease: Charcot-Marie-Tooth disease, Type 4B1
Charcot-Marie-Tooth disease, Type 4B1 		5 0 1 0.20 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 1 0.11 0 0
CUI: C0270912
Disease: Charcot-Marie-Tooth Disease, Type Ib
Charcot-Marie-Tooth Disease, Type Ib 		12 0 1 8.3E-02 0 0
CUI: C0398794
Disease: Hypopigmentation-immunodeficiency disease
Hypopigmentation-immunodeficiency disease 		14 0 1 7.1E-02 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 0 1 7.1E-02 0 0
CUI: C3711383
Disease: Early-Onset Glaucoma
Early-Onset Glaucoma 		15 0 1 6.7E-02 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 1 4.8E-02 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 1 4.8E-02 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 1 4.8E-02 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 1 4.8E-02 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 0 1 3.8E-02 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 1 3.6E-02 0 0
CUI: C1858285
Disease: Decreased number of peripheral myelinated nerve fibers
Decreased number of peripheral myelinated nerve fibers 		28 0 1 3.6E-02 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 1 2.4E-02 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 2.2E-02 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		51 0 1 2.0E-02 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 0 1 1.9E-02 0 0
CUI: C0221373
Disease: Claw hand
Claw hand 		63 0 1 1.6E-02 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 1 1.4E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria 		76 0 1 1.3E-02 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 1 1.2E-02 0 0
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1 		92 0 1 1.1E-02 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 0 1 1.1E-02 0 0