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: C0041651
Disease: Uncomplicated alcohol withdrawal
Uncomplicated alcohol withdrawal 		1 0 1 0.11 0 0
CUI: C0236688
Disease: Cocaine delirium
Cocaine delirium 		1 0 1 0.11 0 0
CUI: C0236701
Disease: Cocaine-induced mood disorder
Cocaine-induced mood disorder 		1 0 1 0.11 0 0
CUI: C0393568
Disease: Vascular parkinsonism
Vascular parkinsonism 		1 0 1 0.11 0 0
CUI: C0425722
Disease: Sexual symptom
Sexual symptom 		1 0 1 0.11 0 0
CUI: C0558089
Disease: Verbally abusive behavior
Verbally abusive behavior 		1 0 1 0.11 0 0
CUI: C0679294
Disease: paternal alcoholism
paternal alcoholism 		1 0 1 0.11 0 0
CUI: C0743072
Disease: Depression, psychotic
Depression, psychotic 		11 0 2 0.11 0 0
CUI: C0947810
Disease: Parkinson's disease and parkinsonism
Parkinson's disease and parkinsonism 		1 0 1 0.11 0 0
CUI: C1829648
Disease: Amino acidemias
Amino acidemias 		1 0 1 0.11 0 0
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME 		11 0 2 0.11 0 0
CUI: C2363747
Disease: Neurological decompensation
Neurological decompensation 		1 0 1 0.11 0 0
CUI: C2363919
Disease: Childhood depression
Childhood depression 		1 0 1 0.11 0 0
CUI: C3280282
Disease: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT 		1 0 1 0.11 0 0
CUI: C3553788
Disease: ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 		1 38 1 0.11 2 5.1E-02
CUI: C3665679
Disease: Undifferentiated attention deficit disorder
Undifferentiated attention deficit disorder 		1 0 1 0.11 0 0
CUI: C4017280
Disease: HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A, DUE TO PARTIAL PTS DEFICIENCY
HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A, DUE TO PARTIAL PTS DEFICIENCY 		1 0 1 0.11 0 0
CUI: C4024976
Disease: Episodic generalized hypotonia
Episodic generalized hypotonia 		1 0 1 0.11 0 0
CUI: C4303546
Disease: Brain dopamine-serotonin vesicular transport disease
Brain dopamine-serotonin vesicular transport disease 		1 0 1 0.11 0 0
CUI: C4310662
Disease: SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE 		1 0 1 0.11 0 0
CUI: C4693325
Disease: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE 		1 0 1 0.11 0 0
CUI: C4693964
Disease: NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE
NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE 		1 0 1 0.11 0 0
CUI: C4747621
Disease: PARKINSONISM-DYSTONIA, INFANTILE, 1
PARKINSONISM-DYSTONIA, INFANTILE, 1 		1 0 1 0.11 0 0
CUI: C4747991
Disease: PARKINSONISM-DYSTONIA, INFANTILE, 2
PARKINSONISM-DYSTONIA, INFANTILE, 2 		1 0 1 0.11 0 0
CUI: C0751093
Disease: Dystonia, Limb
Dystonia, Limb 		42 0 5 0.11 0 0