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: C0025183
Disease: Meige Syndrome
Meige Syndrome
2 0 2 0.50 0 0
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT
5 0 3 0.50 0 0
CUI: C3554447
Disease: DYSTONIA 25
DYSTONIA 25
2 0 2 0.50 0 0
CUI: C0752205
Disease: Dystonia, Secondary
Dystonia, Secondary
10 0 4 0.40 0 0
CUI: C2875058
Disease: Familial torsion dystonia
Familial torsion dystonia
3 0 2 0.40 0 0
Adult-Onset Idiopathic Focal Dystonias
7 0 3 0.38 0 0
Adult-Onset Idiopathic Torsion Dystonias
7 0 3 0.38 0 0
Autosomal Dominant Familial Dystonia
7 0 3 0.38 0 0
Autosomal Recessive Familial Dystonia
7 0 3 0.38 0 0
CUI: C0752206
Disease: Dystonias, Sporadic
Dystonias, Sporadic
7 0 3 0.38 0 0
CUI: C0752208
Disease: Pseudodystonia
Pseudodystonia
7 0 3 0.38 0 0
CUI: C2242579
Disease: Lingual dystonia
Lingual dystonia
4 0 2 0.33 0 0
CUI: C0752202
Disease: Childhood Onset Dystonias
Childhood Onset Dystonias
13 0 4 0.31 0 0
CUI: C0393598
Disease: Idiopathic familial dystonia
Idiopathic familial dystonia
9 0 3 0.30 0 0
CUI: C0752197
Disease: Adult-Onset Dystonias
Adult-Onset Dystonias
9 0 3 0.30 0 0
CUI: C0752207
Disease: Familial Dystonia
Familial Dystonia
15 0 4 0.27 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding)
1 0 1 0.25 0 0
CUI: C3267131
Disease: Psychogenic movement disorder
Psychogenic movement disorder
1 0 1 0.25 0 0
CUI: C3710741
Disease: Torticollis, familial
Torticollis, familial
1 0 1 0.25 0 0
CUI: C4016920
Disease: DYSTONIA 1, TORSION, LATE-ONSET
DYSTONIA 1, TORSION, LATE-ONSET
1 0 1 0.25 0 0
CUI: C0393610
Disease: Dystonia, Diurnal
Dystonia, Diurnal
18 0 4 0.22 0 0
CUI: C0752203
Disease: Dystonia, Primary
Dystonia, Primary
19 0 4 0.21 0 0
CUI: C0266006
Disease: Pili torti-deafness syndrome
Pili torti-deafness syndrome
14 0 3 0.20 0 0
CUI: C0393604
Disease: Isolated blepharospasm
Isolated blepharospasm
2 0 1 0.20 0 0
CUI: C1969807
Disease: Dystonia, Focal, Task-Specific
Dystonia, Focal, Task-Specific
2 0 1 0.20 0 0