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: C0013386
Disease: Dyskinesia, Drug-Induced
Dyskinesia, Drug-Induced 		32 0 15 0.47 0 0
CUI: C0021776
Disease: Intermittent Explosive Disorder
Intermittent Explosive Disorder 		4 0 3 0.19 0 0
CUI: C0454606
Disease: Oral Dyskinesia
Oral Dyskinesia 		7 0 3 0.16 0 0
CUI: C0233612
Disease: Waxy flexibility
Waxy flexibility 		15 0 4 0.15 0 0
CUI: C0266487
Disease: Etat Marbre
Etat Marbre 		23 0 5 0.15 0 0
CUI: C0221480
Disease: Recurrent depression
Recurrent depression 		19 0 4 0.13 0 0
CUI: C4524082
Disease: Segawa syndrome
Segawa syndrome 		2 0 2 0.13 0 0
CUI: C0262376
Disease: anxiety generalized
anxiety generalized 		11 0 3 0.13 0 0
CUI: C3699402
Disease: Alcohol abuse or dependence
Alcohol abuse or dependence 		11 0 3 0.13 0 0
CUI: C4551628
Disease: Opiate Abuse
Opiate Abuse 		12 0 3 0.12 0 0
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement 		22 0 4 0.12 0 0
CUI: C0751217
Disease: Hyperkinesia, Generalized
Hyperkinesia, Generalized 		32 0 5 0.12 0 0
CUI: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium 		23 0 4 0.12 0 0
CUI: C0268467
Disease: Hyperphenylalaninemia, BH4-Deficient, B
Hyperphenylalaninemia, BH4-Deficient, B 		4 0 2 0.12 0 0
CUI: C0596170
Disease: Binge eating disorder
Binge eating disorder 		4 0 2 0.12 0 0
CUI: C1399358
Disease: Hemiparkinsonism
Hemiparkinsonism 		4 0 2 0.12 0 0
CUI: C2673535
Disease: DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)
DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder) 		4 0 2 0.12 0 0
CUI: C0878676
Disease: 6-pyruvoyl-tetrahydropterin synthase deficiency
6-pyruvoyl-tetrahydropterin synthase deficiency 		5 0 2 0.11 0 0
CUI: C0030200
Disease: Pain, Intractable
Pain, Intractable 		6 0 2 0.11 0 0
CUI: C1842534
Disease: DYSTONIA 18 (disorder)
DYSTONIA 18 (disorder) 		6 0 2 0.11 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 4 0.10 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 4 0.10 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 4 0.10 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 4 0.10 0 0
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia 		28 0 4 0.10 0 0