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: C0751776
Disease: Atypical Inclusion-Body Disease
Atypical Inclusion-Body Disease
17 0 17 1.00 0 0
CUI: C0751780
Disease: Biotin-Responsive Encephalopathy
Biotin-Responsive Encephalopathy
17 0 17 1.00 0 0
CUI: C0751782
Disease: May-White Syndrome
May-White Syndrome
17 0 17 1.00 0 0
Action Myoclonus-Renal Failure Syndrome
20 0 17 0.85 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive
48 0 17 0.35 0 0
Dentatorubral-Pallidoluysian Atrophy
95 0 17 0.18 0 0
CUI: C0751785
Disease: Unverricht-Lundborg Syndrome
Unverricht-Lundborg Syndrome
56 0 10 0.16 0 0
CUI: C0751784
Disease: Lafora Body Disease, Late Onset
Lafora Body Disease, Late Onset
2 0 2 0.12 0 0
CUI: C1850764
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC 2B
EPILEPSY, PROGRESSIVE MYOCLONIC 2B
2 0 2 0.12 0 0
CUI: C4317153
Disease: Simple partial occipital seizures
Simple partial occipital seizures
2 0 2 0.12 0 0
CUI: C4476619
Disease: Poor visual behavior for age
Poor visual behavior for age
2 0 2 0.12 0 0
CUI: C4476727
Disease: Erratic myoclonus
Erratic myoclonus
3 0 2 0.11 0 0
CUI: C1849186
Disease: Severe photosensitivity
Severe photosensitivity
4 0 2 0.11 0 0
Giant somatosensory evoked potentials
4 0 2 0.11 0 0
CUI: C0796206
Disease: Atkin syndrome
Atkin syndrome
5 0 2 1.0E-01 0 0
CUI: C0917808
Disease: Vegetative State
Vegetative State
5 0 2 1.0E-01 0 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure
17 0 3 9.7E-02 0 0
CUI: C1850765
Disease: Visual auras
Visual auras
7 0 2 9.1E-02 0 0
CUI: C0742035
Disease: Cerebellar lesion NOS
Cerebellar lesion NOS
9 0 2 8.3E-02 0 0
CUI: C0747651
Disease: Recurrent aspiration pneumonia
Recurrent aspiration pneumonia
11 0 2 7.7E-02 0 0
Complex partial seizure with impairment of consciousness
41 0 4 7.4E-02 0 0
CUI: C1849156
Disease: Spastic Ataxia
Spastic Ataxia
28 0 3 7.1E-02 0 0
SPINOCEREBELLAR ATAXIA 31 (disorder)
13 0 2 7.1E-02 0 0
Photosensitive tonic-clonic seizures
14 0 2 6.9E-02 0 0
CUI: C3698239
Disease: Cerebral cortex myoclonus
Cerebral cortex myoclonus
14 0 2 6.9E-02 0 0