Movement disorder

Part of

Sub-types of Movement disorder

• Extrapyramidal and movement disease 0 trials · 149 incl. sub-types
  1 sub-type

  • Dystonic disorder 65 trials · 149 incl. sub-types Sub-types →
• Cerebellar ataxia 40 trials · 144 incl. sub-types
  1 sub-type

  • Hereditary cerebellar ataxia 0 trials · 116 incl. sub-types Sub-types →
• Multiple system atrophy 110 trials · 119 incl. sub-types
  4 sub-types

  • Pure autonomic failure 18 trials
  • Multiple system atrophy, parkinsonian type 12 trials
  • Multiple system atrophy, cerebellar type 3 trials
  • Striatonigral degeneration 0 trials Sub-types →
• Essential tremor 102 trials · 104 incl. sub-types
  6 sub-types

  • Tremor, hereditary essential, 1 2 trials
  • Tremor, hereditary essential, 2 0 trials
  • Tremor, hereditary essential, 3 0 trials
  • Tremor, hereditary essential, 4 0 trials
  • Tremor, hereditary essential, 5 0 trials
  • Tremor, hereditary essential, 6 0 trials
• Progressive supranuclear palsy 74 trials · 78 incl. sub-types
  4 sub-types

  • Supranuclear palsy, progressive, 1 5 trials
  • Atypical progressive supranuclear palsy syndrome 1 trial · 4 incl. sub-types Sub-types →
  • Supranuclear palsy, progressive, 2 0 trials
  • Supranuclear palsy, progressive, 3 0 trials
• Huntington disease 76 trials
  2 sub-types

  • Juvenile Huntington disease 1 trial
  • Westphal disease 0 trials
• Progressive non-fluent aphasia 24 trials · 44 incl. sub-types
  1 sub-type

  • Semantic dementia 32 trials Sub-types →
• Behavioral variant of frontotemporal dementia 22 trials · 42 incl. sub-types
  3 sub-types

  • Semantic dementia 32 trials Sub-types →
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 7 0 trials
• Tourette syndrome 41 trials
• Corticobasal syndrome 20 trials
• Frontotemporal dementia with motor neuron disease 14 trials · 19 incl. sub-types
  7 sub-types

  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 1 5 trials
  • Amyotrophic lateral sclerosis type 10 3 trials
  • Amyotrophic lateral sclerosis type 6 1 trial
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 0 trials
• Chronic tic disorder 15 trials
• Choreatic disease 11 trials
  5 sub-types

  • Chorea gravidarum 0 trials
  • Chorea, benign familial 0 trials
  • Chorea, remitting, with nystagmus and cataract 0 trials
  • Choreoathetosis, familial inverted 0 trials
  • Hereditary progressive chorea without dementia 0 trials
• Neurodegeneration with brain iron accumulation 1 trial · 8 incl. sub-types
  14 sub-types

  • Neurodegeneration with brain iron accumulation 5 4 trials
  • Pantothenate kinase-associated neurodegeneration 4 trials Sub-types →
  • PLA2G6-associated neurodegeneration 1 trial Sub-types →
  • Kufor-Rakeb syndrome 0 trials Sub-types →
  • Woodhouse-Sakati syndrome 0 trials
  • Aceruloplasminemia 0 trials
  • Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome 0 trials
  • Fatty acid hydroxylase-associated neurodegeneration 0 trials
  • Neurodegeneration with brain iron accumulation 4 0 trials
  • Neurodegeneration with brain iron accumulation 6 0 trials
  • Neurodegeneration with brain iron accumulation 7 0 trials
  • Neurodegeneration with brain iron accumulation 8 0 trials
  • Neurodegeneration with brain iron accumulation 9 0 trials
  • Neuroferritinopathy 0 trials
• Arthrogryposis 4 trials · 6 incl. sub-types
  5 sub-types

  • Freeman-Sheldon syndrome 1 trial Sub-types →
  • Congenital contractural arachnodactyly 1 trial
  • Boylan dew greco syndrome 0 trials
  • Distal arthrogryposis Moore weaver type 0 trials
  • Massa casaer ceulemans syndrome 0 trials
• Inherited Creutzfeldt-Jakob disease 5 trials
• Primary orthostatic tremor 5 trials
• Clonic hemifacial spasm 4 trials
• Familial congenital mirror movements 3 trials
  4 sub-types

  • Mirror movements 1 and/or agenesis of the corpus callosum 0 trials Sub-types →
  • Mirror movements 2 0 trials
  • Mirror movements 3 0 trials
  • Mirror movements 4 0 trials
• Transient tic disorder 3 trials
• Dyskinesia with orofacial involvement, autosomal dominant 2 trials
• Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome 2 trials
• Opsoclonus-myoclonus syndrome 2 trials
• Lafora disease 1 trial
  2 sub-types

  • Myoclonic epilepsy of Lafora 1 0 trials
  • Myoclonic epilepsy of Lafora 2 0 trials
• Unverricht-Lundborg syndrome 1 trial
• Benign shuddering attacks 1 trial
• Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1 trial
• Myoclonus, familial 1 trial
  2 sub-types

  • Myoclonus, familial, 1 0 trials
  • Myoclonus, familial, 2 0 trials
• Neuronal intranuclear inclusion disease 1 trial
• Psychogenic movement disorders 1 trial
• PRRT2-associated paroxysmal movement disorder 0 trials · 1 incl. sub-types
  3 sub-types

  • Episodic kinesigenic dyskinesia 1 1 trial
  • Infantile convulsions and choreoathetosis 0 trials
  • Seizures, benign familial infantile, 2 0 trials
• Intellectual disability-hyperkinetic movement-truncal ataxia syndrome 0 trials · 1 incl. sub-types
  1 sub-type

  • Autosomal recessive limb-girdle muscular dystrophy type R18 1 trial
• Huntington disease-like 3 0 trials
• Huntington disease-like syndrome due to C9ORF72 expansions 0 trials
• SLC6A3-related dopamine transporter deficiency syndrome 0 trials
  2 sub-types

  • Atypical dopamine transporter deficiency syndrome 0 trials
  • Classic dopamine transporter deficiency syndrome 0 trials
• Sandifer syndrome 0 trials
• Benign paroxysmal tonic upgaze of childhood with ataxia 0 trials
• Brain-lung-thyroid syndrome 0 trials
• Childhood-onset benign chorea with striatal involvement 0 trials
• Complex movement disorder with or without neurodevelopmental features 0 trials
  1 sub-type

  • Torsion dystonia 2 0 trials
• Epilepsy with myoclonic absences 0 trials
• Hereditary geniospasm 0 trials
• Hyperekplexia 0 trials
  2 sub-types

  • Hereditary hyperekplexia 0 trials Sub-types →
  • Sporadic hyperekplexia 0 trials
• Isolated facial myokymia 0 trials
• Kuru 0 trials
• Lingual-facial-buccal dyskinesia 0 trials
• Neuroacanthocytosis 0 trials
  2 sub-types

  • VPS13A-related neurodegenerative disease 0 trials
  • XK-related neurodegenerative disease 0 trials
• Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome 0 trials
• Progressive myoclonic epilepsy type 7 0 trials
• Proximal myopathy with extrapyramidal signs 0 trials
• Sensorineural hearing loss-early graying-essential tremor syndrome 0 trials
• Spinal muscular atrophy-progressive myoclonic epilepsy syndrome 0 trials
• Tremor-nystagmus-duodenal ulcer syndrome 0 trials
• Variably protease-sensitive prionopathy 0 trials