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: 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: C0025183
Disease: Meige Syndrome
Meige Syndrome 		2 0 2 0.50 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
CUI: C2749929
Disease: Musician's Dystonia
Musician's Dystonia 		2 0 1 0.20 0 0
CUI: C3554447
Disease: DYSTONIA 25
DYSTONIA 25 		2 0 2 0.50 0 0
CUI: C4524082
Disease: Segawa syndrome
Segawa syndrome 		2 0 1 0.20 0 0
CUI: C0026858
Disease: Musculoskeletal Pain
Musculoskeletal Pain 		3 0 1 0.17 0 0
CUI: C0242684
Disease: Hypodynamia
Hypodynamia 		3 0 1 0.17 0 0
CUI: C0751701
Disease: Hypokinesia, Antiorthostatic
Hypokinesia, Antiorthostatic 		3 0 1 0.17 0 0
CUI: C1504405
Disease: Pyramidal Tract Dysfunction
Pyramidal Tract Dysfunction 		3 0 1 0.17 0 0
CUI: C2875058
Disease: Familial torsion dystonia
Familial torsion dystonia 		3 0 2 0.40 0 0
CUI: C2930898
Disease: Benign essential blepharospasm
Benign essential blepharospasm 		3 0 1 0.17 0 0
CUI: C4022403
Disease: Abnormality of the substantia nigra
Abnormality of the substantia nigra 		3 0 1 0.17 0 0
CUI: C0268467
Disease: Hyperphenylalaninemia, BH4-Deficient, B
Hyperphenylalaninemia, BH4-Deficient, B 		4 0 1 0.14 0 0
CUI: C1263855
Disease: Lumbar radiculopathy
Lumbar radiculopathy 		4 0 1 0.14 0 0
CUI: C2242579
Disease: Lingual dystonia
Lingual dystonia 		4 0 2 0.33 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 1 0.14 0 0
CUI: C3697670
Disease: Spinal cord myoclonus
Spinal cord myoclonus 		4 0 1 0.14 0 0
CUI: C4025696
Disease: Paresis of extensor muscles of the big toe
Paresis of extensor muscles of the big toe 		4 0 1 0.14 0 0
CUI: C0231519
Disease: Gegenhalten
Gegenhalten 		5 0 1 0.12 0 0
CUI: C0233608
Disease: Catatonic Rigidity
Catatonic Rigidity 		5 0 1 0.12 0 0