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: C0040485
Disease: Torticollis
Torticollis
55 0 9 0.13 0 0
CUI: C2242577
Disease: Oromandibular dystonia
Oromandibular dystonia
13 0 4 0.13 0 0
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT
5 4 3 0.13 2 0.20
CUI: C0005747
Disease: Blepharospasm
Blepharospasm
44 6 7 0.12 2 0.17
CUI: C0013423
Disease: Dystonia Musculorum Deformans
Dystonia Musculorum Deformans
26 0 5 0.12 0 0
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia
28 0 5 0.11 0 0
CUI: C1868681
Disease: DYSTONIA 12
DYSTONIA 12
9 0 3 0.11 0 0
Parkinsonism with favorable response to dopaminergic medication
21 0 4 0.11 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders
167 37 17 9.9E-02 7 0.18
CUI: C0423082
Disease: Hypometric saccades
Hypometric saccades
13 0 3 9.7E-02 0 0
CUI: C0025183
Disease: Meige Syndrome
Meige Syndrome
2 0 2 9.5E-02 0 0
CUI: C1969807
Disease: Dystonia, Focal, Task-Specific
Dystonia, Focal, Task-Specific
2 0 2 9.5E-02 0 0
CUI: C2749929
Disease: Musician's Dystonia
Musician's Dystonia
2 8 2 9.5E-02 1 6.7E-02
CUI: C3554447
Disease: DYSTONIA 25
DYSTONIA 25
2 0 2 9.5E-02 0 0
CUI: C4524082
Disease: Segawa syndrome
Segawa syndrome
2 0 2 9.5E-02 0 0
CUI: C0427086
Disease: Involuntary Movements
Involuntary Movements
37 0 5 9.4E-02 0 0
CUI: C0015371
Disease: Extrapyramidal Disorders
Extrapyramidal Disorders
27 0 4 9.1E-02 0 0
CUI: C1839130
Disease: Dystonia 3, Torsion, X-Linked
Dystonia 3, Torsion, X-Linked
15 0 3 9.1E-02 0 0
CUI: C2875058
Disease: Familial torsion dystonia
Familial torsion dystonia
3 0 2 9.1E-02 0 0
CUI: C2930898
Disease: Benign essential blepharospasm
Benign essential blepharospasm
3 1 2 9.1E-02 1 0.12
Iron accumulation in globus pallidus
3 0 2 9.1E-02 0 0
Hyperphenylalaninemia, BH4-Deficient, B
4 0 2 8.7E-02 0 0
Dysfunction of lateral corticospinal tracts
4 0 2 8.7E-02 0 0
CUI: C2242579
Disease: Lingual dystonia
Lingual dystonia
4 0 2 8.7E-02 0 0
DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)
4 0 2 8.7E-02 0 0