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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:movement disorder
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Accession:EFO:0004280 term browser browse the term
Definition:Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement. Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions.
Synonyms:exact_synonym: movement disease;   movement disorders;   tardive dyskinesia
 xref: DOID:480;   HP:0100022;   ICD10:G25;   ICD9:333.90;   ICD9:333.99;   MEDGEN:10113;   MESH:D009069;   MONDO:0005395;   MP:0002066;   MedDRA:10028035;   NCI:C116757;   SCTID:60342002;   SNOMEDCT:60342002;   UMLS:C0026650
 external_ontology: disease_has_major_feature EFO:HP:0100022


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  experimental factor 0
    material property 0
      disposition 0
        disease 0
          nervous system disease 0
            movement disorder 0
              Familial cortical myoclonus 0
              Huntington disease + 0
              Huntington disease-like 3 0
              Huntington disease-like syndrome due to C9ORF72 expansions 0
              Lafora disease + 0
              Opsoclonus-Myoclonus Syndrome 0
              PRRT2-associated paroxysmal movement disorder + 0
              Rare genetic movement disorder + 0
              SLC6A3-related dopamine transporter deficiency syndrome + 0
              Stiff-Person syndrome 0
              Tourette syndrome 0
              Unverricht-Lundborg syndrome 0
              arthrogryposis + 0
              behavioral variant of frontotemporal dementia + 0
              benign paroxysmal tonic upgaze of childhood with ataxia 0
              brain-lung-thyroid syndrome 0
              cerebellar ataxia + 0
              childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 0
              chorea + 0
              chronic tic disorder 0
              corticobasal syndrome 0
              dyskinesia with orofacial involvement, autosomal dominant 0
              epilepsy with myoclonic absences 0
              essential tremor + 0
              extrapyramidal and movement disease + 0
              familial congenital mirror movements + 0
              frontotemporal dementia with motor neuron disease + 0
              hereditary geniospasm 0
              hyperekplexia + 0
              infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome 0
              inherited Creutzfeldt-Jakob disease 0
              intellectual disability-hyperkinetic movement-truncal ataxia syndrome + 0
              juvenile myoclonic epilepsy 0
              kuru 0
              multiple system atrophy + 0
              myoclonus, familial 0
              neuroacanthocytosis + 0
              neurodegeneration with brain iron accumulation + 0
              neuronal intranuclear inclusion disease 0
              periodic limb movement disorder 0
              progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome 0
              progressive non-fluent aphasia + 0
              progressive supranuclear palsy + 0
              proximal myopathy with extrapyramidal signs 0
              sensorineural hearing loss-early graying-essential tremor syndrome 0
              spinal muscular atrophy-progressive myoclonic epilepsy syndrome 0
              transient tic disorder 0
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