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: C4022848
Disease: EEG with centrotemporal focal spike waves
EEG with centrotemporal focal spike waves 		5 0 2 0.22 0 0
CUI: C4022855
Disease: Abnormal involuntary eye movements
Abnormal involuntary eye movements 		6 0 2 0.20 0 0
CUI: C0424304
Disease: Inappropriate laughter
Inappropriate laughter 		7 0 2 0.18 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 0.17 0 0
CUI: C0021355
Disease: Infective otitis externa
Infective otitis externa 		1 0 1 0.17 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 0.17 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 0.17 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 0.17 0 0
CUI: C0157680
Disease: Carbuncle/furuncle
Carbuncle/furuncle 		1 0 1 0.17 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 0.17 0 0
CUI: C0238454
Disease: Cavernous Sinus Thrombosis
Cavernous Sinus Thrombosis 		1 0 1 0.17 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 0.17 0 0
CUI: C0259860
Disease: psychiatric emergencies
psychiatric emergencies 		1 0 1 0.17 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 0.17 0 0
CUI: C0578437
Disease: Ischemic foot
Ischemic foot 		1 0 1 0.17 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 0.17 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 0.17 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 0.17 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 0.17 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 0.17 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 0.17 0 0
CUI: C0854328
Disease: Infection due to anaerobic bacteria
Infection due to anaerobic bacteria 		1 0 1 0.17 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 0.17 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 0.17 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 0.17 0 0