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: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 0 22 7.9E-02 0 0
CUI: C4553976
Disease: Urinary Urgency, CTCAE 5
Urinary Urgency, CTCAE 5 		34 0 10 7.8E-02 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 17 7.6E-02 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 23 7.5E-02 0 0
CUI: C1849134
Disease: Impaired vibration sensation in the lower limbs
Impaired vibration sensation in the lower limbs 		39 0 10 7.5E-02 0 0
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		11 0 8 7.5E-02 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition 		40 0 10 7.5E-02 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 18 7.4E-02 0 0
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17 		12 0 8 7.4E-02 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 13 7.3E-02 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes 		28 0 9 7.3E-02 0 0
CUI: C1859606
Disease: Decreased number of large peripheral myelinated nerve fibers
Decreased number of large peripheral myelinated nerve fibers 		14 0 8 7.3E-02 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 21 7.0E-02 0 0
CUI: C0016506
Disease: Foot Deformities
Foot Deformities 		66 0 11 6.9E-02 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 7 6.6E-02 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 17 6.6E-02 0 0
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		75 0 11 6.5E-02 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 7 6.5E-02 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 7 6.5E-02 0 0
CUI: C1843663
Disease: Urinary bladder sphincter dysfunction
Urinary bladder sphincter dysfunction 		28 0 8 6.5E-02 0 0
CUI: C1833308
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V 		12 0 7 6.4E-02 0 0
CUI: C3661519
Disease: Hereditary Motor Neuronopathy
Hereditary Motor Neuronopathy 		12 0 7 6.4E-02 0 0
CUI: C1836451
Disease: Distal lower limb amyotrophy
Distal lower limb amyotrophy 		29 0 8 6.4E-02 0 0
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		312 0 25 6.4E-02 0 0
CUI: C0221373
Disease: Claw hand
Claw hand 		63 0 10 6.4E-02 0 0