363847004: Movement observable (observable entity)

SNOMED CT Concept\Observable entity\Clinical history/examination observable (observable entity)\Neurological observable\Movement observable (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

486976015 Movement observable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

770030010 Movement observable (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2719291000005119 træk vedr. bevægelse da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Movement observable (observable entity)	Is a	Neurological observable	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Pallidonigral degeneration	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Dubini's chorea	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Pallidopontonigral degeneration	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Juvenile paralysis agitans of Hunt	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Chorea gravidarum	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Birnbaum's syndrome	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Rheumatic chorea	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	5
Pallidoluysian degeneration	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Pigmentary pallidal degeneration	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Chronic progressive non-hereditary chorea	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Rheumatic chorea without heart involvement	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	5
Westphal-Strumpell syndrome	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	6
Juvenile onset Huntington's disease	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Late onset Huntington's disease	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Akinetic-rigid form of Huntington's disease	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Pallidal degeneration	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Benign hereditary chorea	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Chorea due to systemic lupus erythematosus (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Chorea due to thyrotoxicosis (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Kinesiogenic choreoathetosis	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Toxic chorea (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Paroxysmal nonkinesigenic dyskinesia (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3
Paroxysmal kinesigenic dyskinesia (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3
Choreic cerebral palsy	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
A form of dyskinetic cerebral palsy with a combination of chorea and athetosis; movements are irregular, but twisting and curving.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Huntington disease-like syndrome	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Huntington disease-like 3 is a rare Huntington disease-like syndrome characterized by childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on brain MRI) progressive frontal cortical atrophy and bilateral caudate atrophy.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3
Dissociative neurological symptom disorder co-occurrent with chorea	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia).	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Infection causing chorea (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Chorea due to and following infective disorder (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Chorea co-occurrent and due to dentatorubropallidoluysian degeneration (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3
Infantile Convulsions and paroxysmal ChoreoAthetosis (ICCA) syndrome is a neurological condition characterised by the occurrence of seizures during the first year of life and choreoathetotic dyskinetic attacks during childhood or adolescence.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Acquired choreiform dyspraxia	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	6
A rare genetic neurodegenerative disease characterised by movement disorders, including dystonia, chorea, myoclonus, tremor and rigidity. Associated features are also cognitive and memory impairment, early psychiatric disturbances and behavioural problems.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
A rare genetic human prion disease characterised by adult-onset neurodegenerative manifestations associated with a movement disorder and psychiatric/behavioural disturbances. Patients typically present personality changes, aggressiveness, manias, anxiety and/or depression in conjunction with rapidly progressive cognitive decline (presenting with dysarthria, apraxia, aphasia and eventually leading to dementia) as well as ataxia (manifesting with gait disturbances, unsteadiness, coordination problems), Parkinsonism, myoclonus, and/or chorea. Additional features may include generalised spasticity, seizures, urine incontinence and pyramidal abnormalities. There is evidence the disease is caused by 8 extra octapeptide repeats in the PRNP gene on chromosome 20p13.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Chorea due to and following encephalitis	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3
A rare genetic hyperkinetic movement disorder characterized predominantly by chorea of variable severity, associated with bilateral striatal abnormalities on cerebral MRI. The disease is scarcely progressive, and cognitive performance is preserved in the majority of cases, although mild cognitive delay has also been reported.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Classical pantothenate kinase associated neurodegeneration	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Atypical pantothenate kinase associated neurodegeneration (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
A rare multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, choreoathetosis, progressive spastic diplegia, progressive tapetoretinal degeneration with loss of retinal vessels, and glomerulopathy resulting in death late in the first or early in the second decade of life. Absence of the cerebellar granular layer has been reported. There have been no further descriptions in the literature since 1982.	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	8
Hemichorea	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3
Post-hemiplegic chorea	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Hemichorea due to injury of head (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Hemichorea due to cerebral arteriovenous malformation (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Hemichorea due to abscess of brain (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Hemichorea due to cerebral hemorrhage (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Hemichorea due to neoplasm of brain (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Hemichorea due to cerebral infarction (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	4
Hemichorea due to multiple sclerosis (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Andersen Tawil syndrome (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Chorea due to injury of head (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Chorea following injury	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Movement of foot	Is a	True	Movement observable (observable entity)	Inferred relationship	Some
Fisher's syndrome	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	5
Lacunar ataxic hemiparesis	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Lacunar ataxic hemiparesis of right dominant side	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	5
Lacunar ataxic hemiparesis of left dominant side	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	5
Lacunar ataxic hemiparesis of left nondominant side	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	5
Lacunar ataxic hemiparesis of right nondominant side	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	5
Pure motor lacunar infarction	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	1
Pure sensorimotor lacunar infarction	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	7
Facial palsy House-Brackmann grade V of right facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Facial palsy House-Brackmann grade V of left facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Facial palsy House-Brackmann grade VI of left facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Facial palsy House-Brackmann grade VI of right facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Facial palsy House-Brackmann grade IV of left facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Right facial palsy House-Brackmann grade IV	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Left facial palsy House-Brackmann grade III	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Facial palsy House-Brackmann grade III of right facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Facial palsy House-Brackmann grade II of left facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Facial palsy House-Brackmann grade II of right facial nerve (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	2
Progressive external ophthalmoplegia of left eye (disorder)	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3
Right progressive external ophthalmoplegia	Interprets	True	Movement observable (observable entity)	Inferred relationship	Some	3

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Id	Description	Lang	Type	Status	Case?	Module
486976015	Movement observable	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
770030010	Movement observable (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2719291000005119	træk vedr. bevægelse	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)