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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Dyskinesias +     
movement disease +     
Angelman syndrome  
Ataxia +   
Athetosis +   
benign shuddering attacks 
Beta-Ureidopropionase Deficiency  
Bobble-Head Doll Syndrome 
Catalepsy  
choreatic disease +   
cold-induced sweating syndrome +   
congenital mirror movement disorder +   
Drug-Induced Akathisia 
Drug-Induced Dyskinesia +   
Dyskinesia with Orofacial Involvement +   
Dyskinesias +   
Dyskinesias, Seizures, and Intellectual Developmental Disorder  
dystonia +   
A movement disease that is characterized by involuntary muscle contractions causing repetitive or twisting movements. (DO)
extrapyramidal and movement disease  
Familial Infantile Convulsions and Paroxysmal Choreoathetosis  
FETAL AKINESIA, RESPIRATORY INSUFFICIENCY, MICROCEPHALY, POLYMICROGYRIA, AND DYSMORPHIC FACIES  
guanidinoacetate methyltransferase deficiency  
Hyperkinesis +   
Hypokinesia +   
Infantile-Onset Limb and Orofacial Dyskinesia  
lingual-facial-buccal dyskinesia 
Microcephaly Pontocerebellar Hypoplasia Dyskinesia 
Mirror Movements 1  
Mirror Movements 2  
Mirror Movements 3  
Mirror Movements 4  
multiple system atrophy +   
Myoclonus +   
neurodevelopmental disorder with involuntary movements  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND MOVEMENT ABNORMALITIES  
Non-Lissencephalic Cortical Dysplasia 
pantothenate kinase-associated neurodegeneration  
Parkinsonism +   
Paroxysmal Exertion-Induced Dyskinesia and Hemolytic Anemia 
progressive supranuclear palsy +   
Pronation-Supination Of The Forearm, Impairment Of 
Psychomotor Agitation +   
Stiff-Person syndrome  
syndromic X-linked intellectual disability type 10  
Synkinesis +  
Telfer Sugar Jaeger Syndrome 
tic disorder +   
Tics  
Tremor +   
Wilson disease +   
 Amyotrophic Dystonic Paraplegia 
 Bilateral Striatal Necrosis with Dystonia  
 childhood-onset dystonia with optic atrophy and basal ganglia abnormalities  
 deafness-dystonia-optic neuronopathy syndrome  
 DOPA-responsive dystonia  
 dopamine transporter deficiency syndrome +   
 dystonia 12  
 dystonia 21 
 dystonia 22, adult-onset  
 dystonia 22, juvenile-onset  
 dystonia 28, childhood-onset  
 dystonia 30  
 dystonia 31  
 dystonia 32  
 dystonia 33  
 dystonia 35, childhood-onset  
 dystonia 37, early-onset with striatal lesions  
 dystonia 9  
 Dystonia with Cerebellar Atrophy 
 Dystonia with Ringbinden 
 early-onset dystonia and/or spastic paraplegia  
 Episodic Kinesigenic Dyskinesia +   
 episodic kinesigenic dyskinesia 3  
 focal dystonia +   
 generalized dystonia +   
 glucose transporter type 1 deficiency syndrome 2  
 hypermanganesemia with dystonia +   
 Juvenile-Onset Dystonia  
 Leber hereditary optic neuropathy and dystonia  
 Leukoencephalopathy with Dystonia and Motor Neuropathy  
 Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum  
 Mitochondrial Dystonia  
 multifocal dystonia +   
 myoclonic dystonia +   
 NEURODEVELOPMENTAL DISORDER WITH ABSENT SPEECH AND MOVEMENT AND BEHAVIORAL ABNORMALITIES  
 NEURODEVELOPMENTAL DISORDER WITH DYSTONIA AND SEIZURES  
 Parkinson's disease 14  
 paroxysmal nonkinesigenic dyskinesia 1  
 paroxysmal nonkinesigenic dyskinesia 2 
 paroxysmal nonkinesigenic dyskinesia 3  
 Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome  
 Segawa Syndrome, Autosomal Recessive  
 segmental dystonia +   
 sepiapterin reductase deficiency  
 Siddiqi syndrome  
 torsion dystonia 17 

Synonyms
Exact Synonyms: Autosomal Recessive Familial Dystonia ;   Childhood Onset Dystonia ;   Dystonia Disorder ;   Dystonic Disorder ;   Dystonic Disorders ;   Familial Dystonia ;   Familial Dystonias ;   Hereditary Dystonia ;   Hereditary Dystonias ;   Idiopathic Familial Dystonia
Narrow Synonyms: TSPOAP1-RELATED DYSTONIA ;   dystonia 1 ;   regression of motor development with severe dystonia and corresponding basal ganglia lesions
Related Synonyms: Dystonia 1, torsion, modifier of
Primary IDs: MESH:D004421
Alternate IDs: MESH:D020821
Xrefs: ICD10CM:G24 ;   MIM:PS128100 ;   MIM:PS128200 ;   NCI:C34563
Definition Sources: https://rarediseases.org/rare-diseases/dystonia/ "DO" "DO", https://www.mayoclinic.org/diseases-conditions/dystonia/symptoms-causes/syc-20350480 "DO" "DO"

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