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: C0233608
Disease: Catatonic Rigidity
Catatonic Rigidity 		5 0 1 0.12 0 0
CUI: C0239325
Disease: Extensor Rigidity
Extensor Rigidity 		5 0 1 0.12 0 0
CUI: C0277821
Disease: Extrapyramidal Rigidity
Extrapyramidal Rigidity 		5 0 1 0.12 0 0
CUI: C0342687
Disease: dopamine beta hydroxylase deficiency
dopamine beta hydroxylase deficiency 		5 0 1 0.12 0 0
CUI: C1851945
Disease: DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT 		5 0 1 0.12 0 0
CUI: C2717866
Disease: Vestibulodynia
Vestibulodynia 		5 0 1 0.12 0 0
CUI: C0751088
Disease: Dyskinesia, Medication-Induced
Dyskinesia, Medication-Induced 		15 0 2 0.12 0 0
CUI: C0265736
Disease: Congenital anomaly of nose
Congenital anomaly of nose 		6 0 1 0.11 0 0
CUI: C1320474
Disease: Nuchal Rigidity
Nuchal Rigidity 		6 0 1 0.11 0 0
CUI: C3279322
Disease: Progressive flexion contractures
Progressive flexion contractures 		6 0 1 0.11 0 0
CUI: C0393610
Disease: Dystonia, Diurnal
Dystonia, Diurnal 		18 0 2 1.0E-01 0 0
CUI: C0751435
Disease: Hyperphenylalaninaemia
Hyperphenylalaninaemia 		30 38 3 9.7E-02 1 2.0E-02
CUI: C0264162
Disease: Camptocormia
Camptocormia 		8 0 1 9.1E-02 0 0
CUI: C0743332
Disease: Focal Dystonia
Focal Dystonia 		21 0 2 8.7E-02 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 2 8.7E-02 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 0 1 8.3E-02 0 0
CUI: C0008043
Disease: Chiari-Frommel Syndrome
Chiari-Frommel Syndrome 		9 0 1 8.3E-02 0 0
CUI: C0011251
Disease: Delusional disorder
Delusional disorder 		9 0 1 8.3E-02 0 0
CUI: C0086768
Disease: Pancreatic Cholera
Pancreatic Cholera 		9 0 1 8.3E-02 0 0
CUI: C0155668
Disease: Old myocardial infarction
Old myocardial infarction 		9 0 1 8.3E-02 0 0
CUI: C1868681
Disease: DYSTONIA 12
DYSTONIA 12 		9 0 1 8.3E-02 0 0
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		9 0 1 8.3E-02 0 0
CUI: C0752205
Disease: Dystonia, Secondary
Dystonia, Secondary 		10 0 1 7.7E-02 0 0
CUI: C1291316
Disease: Deficiency of reductase
Deficiency of reductase 		10 0 1 7.7E-02 0 0
CUI: C1869117
Disease: Paroxysmal nonkinesigenic dyskinesia
Paroxysmal nonkinesigenic dyskinesia 		10 0 1 7.7E-02 0 0