OMOP Concept 375800
Dystonia
StandardConditionSNOMED15802004Disorder
Maps from
39
Descendants
135
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
39 source codes normalize to Dystonia via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Dystonia across source vocabularies.
- distonía
- distonía (trastorno)
- Dystonia disorder
- Dystonia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
Narrower concepts
(135)Included automatically when you query with descendants.
- 1Adult-onset dystonia parkinsonism
- 1Ataxia telangiectasia variant
- 1Brain dopamine-serotonin vesicular transport disease
- 1Cerebellar ataxia with oculomotor apraxia type 4
- 1Childhood-onset basal ganglia degeneration syndrome
- 1Cranial dystonia
- 1Dissociative neurological symptom disorder co-occurrent with dystonia
- 1Diurnal dystonia
- 1Dopamine transporter deficiency syndrome
- 1Drug-induced dystonia
- 1Dystonia 16
- 1Dystonia due to cerebral anoxia
- 1Dystonia due to disorder of peripheral nervous system
- 1Dystonia due to encephalitis
- 1Dystonia due to familial basal ganglia calcifications
- 1Dystonia due to focal brain lesion
- 1Dystonia due to glutaric acidemia
- 1Dystonia due to head injury
- 1Dystonia due to hereditary disease
- 1Dystonia due to homocystinuria
- 1Dystonia due to mitochondrial disease
- 1Dystonia due to neutral 1 amino acid transport defect
- 1Dystonia lenticularis
- 1Dystonic cerebral palsy
- 1Exacerbation of dystonia
- 1Focal dystonia
- 1Fragments of torsion dystonia
- 1Functional dystonia
- 1Generalized dystonia
- 1Hemidystonia
- 1Huntington's chorea
- 1Hypermanganesemia with dystonia
- 1Hyperphenylalaninemia due to DNAJC12 deficiency
- 1Infantile epileptic dyskinetic encephalopathy
- 1Infantile-onset generalized dyskinesia with orofacial involvement
- 1IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome
- 1Maternally inherited mitochondrial dystonia
- 1Myoclonic dystonia
- 1Occupational dystonia
- 1Paroxysmal dystonia
- 1Posthemiplegic dystonia
- 1Primary dystonia DYT27 type
- 1Progressive myoclonic epilepsy with dystonia
- 1Rapid onset dystonia parkinsonism
- 1Segmental dystonia
- 1Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
- 1Sleep-related dystonia
- 1Torsion dystonia
- 1Toxic dystonia
- 1X-linked dystonia parkinsonism
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