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: C1856691
Disease: Impaired proprioception
Impaired proprioception 		15 0 2 0.13 0 0
CUI: C0232766
Disease: Asterixis
Asterixis 		7 0 1 0.12 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		7 0 1 0.12 0 0
CUI: C0454606
Disease: Oral Dyskinesia
Oral Dyskinesia 		7 0 1 0.12 0 0
CUI: C0752196
Disease: Ballismus
Ballismus 		7 0 1 0.12 0 0
CUI: C1838027
Disease: Incomprehensible speech
Incomprehensible speech 		7 0 1 0.12 0 0
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		8 0 1 0.11 0 0
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		8 0 1 0.11 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 1 0.11 0 0
CUI: C0221169
Disease: Hemiballismus
Hemiballismus 		9 0 1 1.0E-01 0 0
CUI: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 1 1.0E-01 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 1 9.1E-02 0 0
CUI: C1853767
Disease: Impaired distal vibration sensation
Impaired distal vibration sensation 		10 0 1 9.1E-02 0 0
CUI: C0020440
Disease: Hypercapnia
Hypercapnia 		11 0 1 8.3E-02 0 0
CUI: C0023009
Disease: Speech and language disorder
Speech and language disorder 		11 0 1 8.3E-02 0 0
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		11 0 1 8.3E-02 0 0
CUI: C0393519
Disease: Cerebellar Ataxia, Early Onset
Cerebellar Ataxia, Early Onset 		12 0 1 7.7E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3 		12 0 1 7.7E-02 0 0
CUI: C1519787
Disease: Undifferentiated Neuroblastoma
Undifferentiated Neuroblastoma 		12 0 1 7.7E-02 0 0
CUI: C4551628
Disease: Opiate Abuse
Opiate Abuse 		12 0 1 7.7E-02 0 0
CUI: C1861736
Disease: SPINOCEREBELLAR ATAXIA 31 (disorder)
SPINOCEREBELLAR ATAXIA 31 (disorder) 		13 0 1 7.1E-02 0 0
CUI: C3276549
Disease: OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY 		14 0 1 6.7E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 2 6.5E-02 0 0
CUI: C0751088
Disease: Dyskinesia, Medication-Induced
Dyskinesia, Medication-Induced 		15 0 1 6.2E-02 0 0
CUI: C1849148
Disease: Decreased sensory nerve conduction velocity
Decreased sensory nerve conduction velocity 		15 0 1 6.2E-02 0 0