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: C0751785
Disease: Unverricht-Lundborg Syndrome
Unverricht-Lundborg Syndrome 		56 17 33 0.46 5 0.17
CUI: C0751779
Disease: Action Myoclonus-Renal Failure Syndrome
Action Myoclonus-Renal Failure Syndrome 		20 20 18 0.36 1 2.8E-02
CUI: C0751776
Disease: Atypical Inclusion-Body Disease
Atypical Inclusion-Body Disease 		17 0 17 0.35 0 0
CUI: C0751777
Disease: Familial Progressive Myoclonic Epilepsy
Familial Progressive Myoclonic Epilepsy 		17 0 17 0.35 0 0
CUI: C0751780
Disease: Biotin-Responsive Encephalopathy
Biotin-Responsive Encephalopathy 		17 0 17 0.35 0 0
CUI: C0751782
Disease: May-White Syndrome
May-White Syndrome 		17 0 17 0.35 0 0
CUI: C0751781
Disease: Dentatorubral-Pallidoluysian Atrophy
Dentatorubral-Pallidoluysian Atrophy 		95 0 21 0.17 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		71 0 15 0.14 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		35 0 7 9.2E-02 0 0
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		13 0 5 8.9E-02 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 34 25 8.7E-02 1 2.0E-02
CUI: C0028968
Disease: Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies 		28 0 6 8.6E-02 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 8 12 8.5E-02 1 4.2E-02
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 7 8.0E-02 0 0
CUI: C0270816
Disease: epilepsy and migraine
epilepsy and migraine 		7 0 4 7.8E-02 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor 		95 0 10 7.5E-02 0 0
CUI: C4281802
Disease: Spongiform encephalopathy
Spongiform encephalopathy 		14 0 4 6.9E-02 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease 		92 32 9 6.9E-02 1 2.1E-02
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 5 6.8E-02 0 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure 		17 0 4 6.6E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 4 6.5E-02 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 11 6.4E-02 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 8 6.3E-02 0 0
CUI: C2676254
Disease: Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia
Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia 		3 0 3 6.2E-02 0 0
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 0 4 6.2E-02 0 0