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: C0751776
Disease: Atypical Inclusion-Body Disease
Atypical Inclusion-Body Disease 		17 0 17 0.85 0 0
CUI: C0751777
Disease: Familial Progressive Myoclonic Epilepsy
Familial Progressive Myoclonic Epilepsy 		17 0 17 0.85 0 0
CUI: C0751780
Disease: Biotin-Responsive Encephalopathy
Biotin-Responsive Encephalopathy 		17 0 17 0.85 0 0
CUI: C0751782
Disease: May-White Syndrome
May-White Syndrome 		17 0 17 0.85 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		48 17 18 0.36 1 2.8E-02
CUI: C0751781
Disease: Dentatorubral-Pallidoluysian Atrophy
Dentatorubral-Pallidoluysian Atrophy 		95 0 17 0.17 0 0
CUI: C0751785
Disease: Unverricht-Lundborg Syndrome
Unverricht-Lundborg Syndrome 		56 0 11 0.17 0 0
CUI: C0747651
Disease: Recurrent aspiration pneumonia
Recurrent aspiration pneumonia 		11 0 3 0.11 0 0
CUI: C0751784
Disease: Lafora Body Disease, Late Onset
Lafora Body Disease, Late Onset 		2 0 2 1.0E-01 0 0
CUI: C1850764
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC 2B
EPILEPSY, PROGRESSIVE MYOCLONIC 2B 		2 0 2 1.0E-01 0 0
CUI: C4317153
Disease: Simple partial occipital seizures
Simple partial occipital seizures 		2 0 2 1.0E-01 0 0
CUI: C4476619
Disease: Poor visual behavior for age
Poor visual behavior for age 		2 0 2 1.0E-01 0 0
CUI: C4476727
Disease: Erratic myoclonus
Erratic myoclonus 		3 0 2 9.5E-02 0 0
CUI: C1849186
Disease: Severe photosensitivity
Severe photosensitivity 		4 0 2 9.1E-02 0 0
CUI: C3806961
Disease: Giant somatosensory evoked potentials
Giant somatosensory evoked potentials 		4 0 2 9.1E-02 0 0
CUI: C0595948
Disease: Atypical absence seizure
Atypical absence seizure 		17 0 3 8.8E-02 0 0
CUI: C0796206
Disease: Atkin syndrome
Atkin syndrome 		5 0 2 8.7E-02 0 0
CUI: C0917808
Disease: Vegetative State
Vegetative State 		5 0 2 8.7E-02 0 0
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		71 9 7 8.3E-02 1 3.6E-02
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder) 		6 0 2 8.3E-02 0 0
CUI: C0751354
Disease: Myoclonus, Action
Myoclonus, Action 		6 0 2 8.3E-02 0 0
CUI: C0428465
Disease: Serum lipids high (finding)
Serum lipids high (finding) 		7 0 2 8.0E-02 0 0
CUI: C1850765
Disease: Visual auras
Visual auras 		7 0 2 8.0E-02 0 0
CUI: C0742035
Disease: Cerebellar lesion NOS
Cerebellar lesion NOS 		9 0 2 7.4E-02 0 0
CUI: C1838681
Disease: Rapidly progressive
Rapidly progressive 		38 0 4 7.4E-02 0 0