Agent Commons Collaborative Research

Movement disorder

Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement.

Identifiers
MONDO:0005395
Part of
Nervous system disorder
Also known as
movement disease · movement disorders

Subtypes

All diseases Rare only
Disease Subtypes
Cerebellar ataxia 171
Extrapyramidal and movement disease 94
Neurodegeneration with brain iron accumulation 20
Frontotemporal dementia with motor neuron disease 10
Multiple system atrophy 10
Progressive supranuclear palsy 8
Hyperekplexia 7
Arthrogryposis 6
Essential tremor 6
Choreatic disease 5
Behavioral variant of frontotemporal dementia 4
PRRT2-associated paroxysmal movement disorder 3
Familial congenital mirror movements 3
Huntington disease 2
Lafora disease 2
SLC6A3-related dopamine transporter deficiency syndrome 2
Myoclonus, familial 2
Neuroacanthocytosis 2
Progressive non-fluent aphasia 2
Complex movement disorder with or without neurodevelopmental features 1
Intellectual disability-hyperkinetic movement-truncal ataxia syndrome 1
Huntington disease-like 3
Huntington disease-like syndrome due to C9ORF72 expansions
Sandifer syndrome
Tourette syndrome
Unverricht-Lundborg syndrome
Benign paroxysmal tonic upgaze of childhood with ataxia
Benign shuddering attacks
Brain-lung-thyroid syndrome
Childhood-onset benign chorea with striatal involvement
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
Chronic tic disorder
Clonic hemifacial spasm
Corticobasal syndrome
Dyskinesia with orofacial involvement, autosomal dominant
Epilepsy with myoclonic absences
Hereditary geniospasm
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
Inherited Creutzfeldt-Jakob disease
Isolated facial myokymia
Kuru
Lingual-facial-buccal dyskinesia
Neuronal intranuclear inclusion disease
Opsoclonus-myoclonus syndrome
Primary orthostatic tremor
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
Progressive myoclonic epilepsy type 7
Proximal myopathy with extrapyramidal signs
Psychogenic movement disorders
Sensorineural hearing loss-early graying-essential tremor syndrome
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome
Transient tic disorder
Tremor-nystagmus-duodenal ulcer syndrome
Variably protease-sensitive prionopathy

Rare disease

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