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Ontology Browser

Parent Terms Term With Siblings Child Terms
Dyskinesias +     
movement disease +     
Akathisia, Drug-Induced 
Angelman syndrome  
Ataxia +   
Athetosis +   
benign shuddering attacks 
Beta-Ureidopropionase Deficiency  
Bobble-Head Doll Syndrome 
choreatic disease +   
cold-induced sweating syndrome +   
congenital mirror movement disorder +   
Drug-Induced Dyskinesia +   
Dyskinesias +   
Dyskinesias, Seizures, and Intellectual Developmental Disorder  
dystonia +   
An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77)
extrapyramidal and movement disease 
Familial Dyskinesia with Facial Myokymia  
Familial Infantile Convulsions and Paroxysmal Choreoathetosis  
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 +   
Non-Lissencephalic Cortical Dysplasia 
pantothenate kinase-associated neurodegeneration +   
Parkinsonian Disorders +   
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 +   
Tremor +   
Wilson disease +   

Exact Synonyms: Adult Onset Idiopathic Torsion Dystonias ;   Autosomal Dominant Familial Dystonia ;   Autosomal Recessive Familial Dystonia ;   Childhood Onset Dystonia ;   Childhood Onset Dystonias ;   Dystonia Disorder ;   Dystonia Disorders ;   Dystonic Disorder ;   Dystonic Disorders ;   Familial Dystonia ;   Familial Dystonias ;   Hereditary Dystonia ;   Hereditary Dystonias ;   Idiopathic Familial Dystonia ;   Idiopathic Familial Dystonias ;   Limb Dystonia ;   Muscle Dystonia ;   Primary Dystonia ;   Primary Dystonias ;   Pseudodystonia ;   Pseudodystonias ;   Psychogenic Dystonia ;   Psychogenic Dystonias ;   Secondary Dystonia ;   Secondary Dystonias ;   Sporadic Dystonia ;   Sporadic Dystonias ;   adult onset dystonias ;   adult onset idiopathic focal dystonias ;   adult-onset dystonia ;   diurnal dystonia ;   dystonic disease ;   paroxysmal dystonia ;   writer cramp ;   writer's cramp ;   writers cramp
Narrow Synonyms: 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 ;   MESH:D020821
Alternate IDs: DOID:9007625 ;   RDO:0000640 ;   RDO:0000641
Xrefs: ICD10CM:G24 ;   ICD10CM:G24.9 ;   NCI:C34563 ;   OMIM:PS128100 ;   OMIM:PS128200
Definition Sources: MESH:D004421

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.