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: C0750951
Disease: Lenticulostriate Disorders
Lenticulostriate Disorders
12 0 12 0.44 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases
19 0 12 0.35 0 0
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM
9 0 5 0.16 0 0
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia
26 0 7 0.15 0 0
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME
11 0 5 0.15 0 0
Primary familial brain calcification
12 0 5 0.15 0 0
CUI: C0012734
Disease: Disruptive Behavior Disorder
Disruptive Behavior Disorder
13 0 5 0.14 0 0
Coenzyme A synthase protein associated neurodegeneration
5 0 4 0.14 0 0
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome
22 0 6 0.14 0 0
Neurodegeneration with brain iron accumulation (NBIA)
40 0 8 0.14 0 0
CUI: C0392156
Disease: Akathisia
Akathisia
15 0 5 0.14 0 0
CUI: C0027849
Disease: Neuroleptic Malignant Syndrome
Neuroleptic Malignant Syndrome
16 0 5 0.13 0 0
CUI: C0854107
Disease: Subcutaneous hemorrhage
Subcutaneous hemorrhage
16 0 5 0.13 0 0
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy
17 0 5 0.13 0 0
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy
17 0 5 0.13 0 0
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
19 0 5 0.12 0 0
CUI: C0393590
Disease: Fahr's syndrome (disorder)
Fahr's syndrome (disorder)
10 0 4 0.12 0 0
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
94 0 13 0.12 0 0
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia
94 0 13 0.12 0 0
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders
20 0 5 0.12 0 0
Dense calcifications in the cerebellar dentate nucleus
3 0 3 0.11 0 0
Calcification of the small brain vessels
3 0 3 0.11 0 0
CUI: C1735368
Disease: Acute dystonia
Acute dystonia
4 0 3 0.11 0 0
DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)
4 0 3 0.11 0 0
Malignancy-associated membranous nephropathy
4 0 3 0.11 0 0