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: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		351 81 72 1.0E-01 3 1.5E-02
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 34 64 1.0E-01 8 5.5E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		1630 348 187 9.9E-02 5 1.1E-02
CUI: C0442874
Disease: Neuropathy
Neuropathy 		484 110 82 9.7E-02 1 4.4E-03
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 		102 0 48 9.7E-02 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 66 9.6E-02 0 0
CUI: C0497327
Disease: Dementia
Dementia 		816 176 110 9.6E-02 5 1.7E-02
CUI: C0427190
Disease: Ataxia, Truncal
Ataxia, Truncal 		68 13 44 9.5E-02 1 7.6E-03
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 95 70 9.4E-02 1 4.7E-03
CUI: C0036572
Disease: Seizures
Seizures 		2152 553 220 9.3E-02 17 2.6E-02
CUI: C0542476
Disease: Forgetful
Forgetful 		429 0 73 9.2E-02 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		167 37 51 9.2E-02 2 1.3E-02
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		454 44 73 8.9E-02 4 2.5E-02
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 42 8.8E-02 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy 		1215 339 134 8.8E-02 8 1.8E-02
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome 		316 42 61 8.8E-02 2 1.3E-02
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		457 64 72 8.7E-02 3 1.7E-02
CUI: C0235031
Disease: Neurologic Symptoms
Neurologic Symptoms 		233 0 54 8.7E-02 0 0
CUI: C0233794
Disease: Memory impairment
Memory impairment 		763 0 96 8.7E-02 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		64 11 40 8.6E-02 3 2.3E-02
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 121 107 8.6E-02 2 8.4E-03
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 10 47 8.6E-02 3 2.4E-02
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		955 164 110 8.6E-02 3 1.1E-02
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		1825 553 178 8.5E-02 12 1.8E-02
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		1075 276 119 8.5E-02 4 1.0E-02