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: C0013423
Disease: Dystonia Musculorum Deformans
Dystonia Musculorum Deformans 		26 0 6 0.16 0 0
CUI: C1851945
Disease: DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT 		5 0 3 0.15 0 0
CUI: C0266006
Disease: Pili torti-deafness syndrome
Pili torti-deafness syndrome 		14 0 4 0.14 0 0
CUI: C1836149
Disease: Axial dystonia
Axial dystonia 		6 0 3 0.14 0 0
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia 		28 0 5 0.12 0 0
CUI: C0025183
Disease: Meige Syndrome
Meige Syndrome 		2 0 2 0.11 0 0
CUI: C3554447
Disease: DYSTONIA 25
DYSTONIA 25 		2 0 2 0.11 0 0
CUI: C4524082
Disease: Segawa syndrome
Segawa syndrome 		2 0 2 0.11 0 0
CUI: C2875058
Disease: Familial torsion dystonia
Familial torsion dystonia 		3 0 2 0.11 0 0
CUI: C3887667
Disease: Retrocollis
Retrocollis 		3 0 2 0.11 0 0
CUI: C0268467
Disease: Hyperphenylalaninemia, BH4-Deficient, B
Hyperphenylalaninemia, BH4-Deficient, B 		4 0 2 1.0E-01 0 0
CUI: C0427086
Disease: Involuntary Movements
Involuntary Movements 		37 0 5 1.0E-01 0 0
CUI: C1839130
Disease: Dystonia 3, Torsion, X-Linked
Dystonia 3, Torsion, X-Linked 		15 0 3 1.0E-01 0 0
CUI: C2242579
Disease: Lingual dystonia
Lingual dystonia 		4 0 2 1.0E-01 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 1.0E-01 0 0
CUI: C0231519
Disease: Gegenhalten
Gegenhalten 		5 0 2 9.5E-02 0 0
CUI: C0233608
Disease: Catatonic Rigidity
Catatonic Rigidity 		5 0 2 9.5E-02 0 0
CUI: C0239325
Disease: Extensor Rigidity
Extensor Rigidity 		5 0 2 9.5E-02 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 4 9.5E-02 0 0
CUI: C0277821
Disease: Extrapyramidal Rigidity
Extrapyramidal Rigidity 		5 0 2 9.5E-02 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 4 9.5E-02 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 4 9.5E-02 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 4 9.5E-02 0 0
CUI: C0878676
Disease: 6-pyruvoyl-tetrahydropterin synthase deficiency
6-pyruvoyl-tetrahydropterin synthase deficiency 		5 0 2 9.5E-02 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		167 0 16 9.5E-02 0 0