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: C0278161
Disease: Ataxia, Motor
Ataxia, Motor 		16 0 16 0.46 0 0
CUI: C0750940
Disease: Tremor, Rubral
Tremor, Rubral 		18 0 16 0.43 0 0
CUI: C0427190
Disease: Ataxia, Truncal
Ataxia, Truncal 		68 0 18 0.21 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination 		59 0 16 0.21 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 19 0.19 0 0
CUI: C0240914
Disease: Romberg's sign positive
Romberg's sign positive 		15 0 5 0.11 0 0
CUI: C0019816
Disease: Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy 		6 0 4 0.11 0 0
CUI: C1832776
Disease: Hypertrophic nerve changes
Hypertrophic nerve changes 		6 0 4 0.11 0 0
CUI: C4021585
Disease: Impaired distal proprioception
Impaired distal proprioception 		7 0 4 0.11 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 4 1.0E-01 0 0
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		26 0 5 8.9E-02 0 0
CUI: C0751122
Disease: Infantile Severe Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy 		63 0 8 8.9E-02 0 0
CUI: C1849148
Disease: Decreased sensory nerve conduction velocity
Decreased sensory nerve conduction velocity 		15 0 4 8.7E-02 0 0
CUI: C1858729
Disease: Decreased motor nerve conduction velocity
Decreased motor nerve conduction velocity 		41 0 6 8.6E-02 0 0
CUI: C0027743
Disease: Nerve compression syndrome
Nerve compression syndrome 		5 0 3 8.1E-02 0 0
CUI: C1510429
Disease: Entrapment Neuropathies
Entrapment Neuropathies 		5 0 3 8.1E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 8 5 7.9E-02 1 0.12
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy 		33 0 5 7.9E-02 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 4 7.7E-02 0 0
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		36 0 5 7.6E-02 0 0
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		23 0 4 7.4E-02 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 0 4 7.0E-02 0 0
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		11 0 3 7.0E-02 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		57 0 6 7.0E-02 0 0
CUI: C4014430
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 		11 0 3 7.0E-02 0 0