movement disorder
Findings
No curated finding names movement disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement.
Definition from the Mondo Disease Ontology (MONDO:0005395), read 2026-09-29. CC BY 4.0.
Features
1 feature
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, hp/releases/2026-09-01.
- Abnormality of movementMondoHP:0100022
Genes
3 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- A kind of
- Narrower terms (54)
- arthrogryposis
- behavioral variant of frontotemporal dementia
- benign paroxysmal tonic upgaze of childhood with ataxia
- benign shuddering attacks
- brain-lung-thyroid syndrome
- cerebellar ataxia
- childhood-onset benign chorea with striatal involvement
- childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
- choreatic disease
- chronic tic disorder
- clonic hemifacial spasm
- complex movement disorder with or without neurodevelopmental features
- corticobasal syndrome
- dyskinesia with orofacial involvement, autosomal dominant
- epilepsy with myoclonic absences
- essential tremor
- extrapyramidal and movement disease
- familial congenital mirror movements
- frontotemporal dementia with motor neuron disease
Other names
2 names
Resolves to: movement disorder
- Also called
- movement diseasemovement disorders