FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term movement disease ID (Ontology) DOID:480 (Human Disease)
Definition A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.
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Spanning Tree (Parents/Children)
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  central nervous system disease
   |__brain disease
       |__movement disease  120 rec.
           |__benign shuddering attacks
           |__choreatic disease 1 rec.
           |   |__chorea gravidarum
           |__congenital mirror movement disorder 6 rec.
           |   |__mirror movements 1 2 rec.
           |   |__mirror movements 2 1 rec.
           |   |__mirror movements 3 1 rec.
           |   |__mirror movements 4 2 rec.
           |__dopamine transporter deficiency syndrome 12 rec.
           |   |__atypical dopamine transporter deficiency syndrome
           |   |__classic dopamine transporter deficiency syndrome 12 rec.
           |__dystonia 77 rec.
           |   |__childhood-onset dystonia with optic atrophy and basal ganglia abnormalities 10 rec.
           |   |__dopa-responsive dystonia 1 rec.
           |   |__dystonia 9 5 rec.
           |   |__dystonia 12 2 rec.
           |   |__dystonia 21
           |   |__dystonia 22, adult-onset 1 rec.
           |   |__dystonia 22, juvenile-onset 1 rec.
           |   |__dystonia 28, childhood-onset 1 rec.
           |   |__dystonia 30 1 rec.
           |   |__dystonia 31 6 rec.
           |   |__dystonia 32 1 rec.
           |   |__dystonia 33 1 rec.
           |   |__dystonia 35, childhood-onset 1 rec.
           |   |__dystonia 37, early-onset with striatal lesions 1 rec.
           |   |__early-onset dystonia and/or spastic paraplegia 4 rec.
           |   |__episodic kinesigenic dyskinesia 1
           |   |__episodic kinesigenic dyskinesia 2
           |   |__episodic kinesigenic dyskinesia 3
           |   |__focal dystonia(+) 2 rec.
           |   |__generalized dystonia(+) 10 rec.
           |   |__glucose transporter type 1 deficiency syndrome 2 5 rec.
           |   |__multifocal dystonia(+) 4 rec.
           |   |__myoclonic dystonia(+) 3 rec.
           |   |__myoclonic dystonia 34 1 rec.
           |   |__paroxysmal nonkinesigenic dyskinesia 1 1 rec.
           |   |__paroxysmal nonkinesigenic dyskinesia 2
           |   |__paroxysmal nonkinesigenic dyskinesia 3 5 rec.
           |   |__segmental dystonia(+)
           |   |__sepiapterin reductase deficiency 2 rec.
           |   |__torsion dystonia 2 1 rec.
           |   |__torsion dystonia 4 4 rec.
           |   |__torsion dystonia 13
           |   |__torsion dystonia 17
           |__essential tremor 12 rec.
           |   |__essential tremor 1 1 rec.
           |   |__essential tremor 2
           |   |__essential tremor 3
           |   |__essential tremor 4 3 rec.
           |   |__essential tremor 5 1 rec.
           |   |__essential tremor 6
           |__extrapyramidal and movement disease 2 rec.
           |__infantile parkinsonism-dystonia 2 1 rec.
           |__lingual-facial-buccal dyskinesia
           |__neurodevelopmental disorder with involuntary movements 1 rec.
           |__Parkinsonism
           |   |__vascular Parkinsonism
           |__progressive supranuclear palsy 7 rec.
           |__Stiff-Person syndrome
           |__X-linked parkinsonism-spasticity syndrome 1 rec.
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MESH:D009069
NCI:C116757
SNOMEDCT_US_2023_03_01:60342002
UMLS_CUI:C0026650