255324009: Movement (observable entity)

SNOMED CT Concept\Observable entity\Process (observable entity)\Movement

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Movement	Is a	Gross motor functions	false	Inferred relationship	Some
Movement	Is a	Process (observable entity)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Extension of right side of sacral spine	Interprets	True	Movement	Inferred relationship	Some	3
Extension of left side of sacral spine	Interprets	True	Movement	Inferred relationship	Some	3
Bilateral sacral extension (finding)	Interprets	True	Movement	Inferred relationship	Some	3
Flexion of left side of sacral spine (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Flexion of right side of sacral spine (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Bilateral sacral flexion (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Injury to a joint due to an extension beyond the normal range of motion	Interprets	True	Movement	Inferred relationship	Some	4
Injury to a joint due to flexion of a joint beyond its normal range of movement.	Interprets	True	Movement	Inferred relationship	Some	4
Propriospinal myoclonus at sleep onset in infancy	Interprets	True	Movement	Inferred relationship	Some	3
Hyperextension injury of finger (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Hyperextension injury of thumb (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Hyperextension injury of neck	Interprets	True	Movement	Inferred relationship	Some	4
Drug-induced dyskinesia	Interprets	True	Movement	Inferred relationship	Some	2
Drug-induced dyskinesia, acute onset	Interprets	True	Movement	Inferred relationship	Some	3
Tardive dyskinesia (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
Neuroleptic-induced tardive dyskinesia	Interprets	True	Movement	Inferred relationship	Some	1
Subacute dyskinesia caused by drug	Interprets	True	Movement	Inferred relationship	Some	1
Paralysis of cervical sympathetic trunk (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Acute mastoiditis with facial paralysis	Interprets	True	Movement	Inferred relationship	Some	4
Rheumatic chorea with heart involvement	Interprets	False	Movement	Inferred relationship	Some	5
Rheumatic chorea	Interprets	False	Movement	Inferred relationship	Some	5
Rheumatic chorea without heart involvement	Interprets	False	Movement	Inferred relationship	Some	5
Tremor due to pheochromocytoma	Interprets	True	Movement	Inferred relationship	Some	2
Parkinsonism	Interprets	True	Movement	Inferred relationship	Some	3
A rare neurodegenerative disease usually presenting before the age of 30 and which is characterized by dystonia, L-dopa-responsive parkinsonism, pyramidal signs and rapid cognitive decline.	Interprets	True	Movement	Inferred relationship	Some	4
Bradykinesia (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder)	Interprets	True	Movement	Inferred relationship	Some	7
Syphilitic parkinsonism	Interprets	True	Movement	Inferred relationship	Some	3
Striatonigral degeneration	Interprets	True	Movement	Inferred relationship	Some	3
Postencephalitic parkinsonism	Interprets	True	Movement	Inferred relationship	Some	4
Juvenile Parkinson's disease	Interprets	True	Movement	Inferred relationship	Some	3
Secondary parkinsonism	Interprets	True	Movement	Inferred relationship	Some	3
Carbon monoxide-induced parkinsonism	Interprets	True	Movement	Inferred relationship	Some	4
Manganese-induced parkinsonism	Interprets	True	Movement	Inferred relationship	Some	4
Parkinsonism with calcification of basal ganglia (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Vascular parkinsonism	Interprets	True	Movement	Inferred relationship	Some	3
Symptomatic parkinsonism	Interprets	True	Movement	Inferred relationship	Some	3
On - off phenomenon (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Impaired psychomotor performance (finding)	Interprets	True	Movement	Inferred relationship	Some	2
A rare neurodegenerative disease characterized by extrapyramidal symptoms (rigidity, tremor, bradykinesia) and dementia, typically beginning in the fifth or sixth decade of life and progressing to a vegetative state with pelvicrural flexion contractures within few years. Oculomotor signs, olfactory dysfunction, and autonomic disturbances may also be observed. Neuropathological hallmarks are frontotemporally accentuated cerebral atrophy, as well as neurofibrillary tangles and neuronal loss in a characteristic distribution in cortical and subcortical regions. The disease is endemic to the Pacific Island of Guam.	Interprets	True	Movement	Inferred relationship	Some	6
Parkinsonism caused by carbon disulfide (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Parkinsonism caused by methanol	Interprets	True	Movement	Inferred relationship	Some	4
X-linked dystonia parkinsonism	Interprets	True	Movement	Inferred relationship	Some	3
Perry syndrome	Interprets	True	Movement	Inferred relationship	Some	3
Abrupt onset of dystonia with parkinsonism over a period of hours to days.	Interprets	True	Movement	Inferred relationship	Some	3
A rare, genetic, neurological disorder characterized by parkinsonian features (including resting or action tremor, cogwheel rigidity, hypomimia and bradykinesia) associated with variably penetrant spasticity, hyperactive deep tendon reflexes and Babinski sign.	Interprets	True	Movement	Inferred relationship	Some	5
A rare parkinsonian syndrome due to intoxication which develops in individuals surviving an acute cyanide intoxication episode or due to chronic exposure to small cyanide doses. It presents several weeks after acute exposure with progressive typical clinical features of parkinsonism including bradykinesia, rigidity, dystonia, hypomimia, hypokinetic dysarthria, postural instability and retropulsion but no resting or postural tremor. Brain MRI reveals bilateral lesions in the pallidum, posterior putamen, substantia nigra, subthalamic nucleus, temporal and occipital cortex, and cerebellum.	Interprets	True	Movement	Inferred relationship	Some	3
Dissociative neurological symptom disorder co-occurrent with parkinsonism (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
A rare neuronal ceroid lipofuscinosis disorder with characteristics of juvenile-onset progressive spinocerebellar ataxia, bulbar syndrome (manifesting with dysarthria, dysphagia and dysphonia), pyramidal and extrapyramidal involvement (including myoclonus, amyotrophy, unsteady gait, akinesia, rigidity, dysarthric speech) and intellectual deterioration. Muscle biopsy displays autofluorescent bodies and lipofuscin deposits in brain and occasionally the retina upon post mortem.	Interprets	True	Movement	Inferred relationship	Some	7
Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder)	Interprets	True	Movement	Inferred relationship	Some	5
Parkinsonism co-occurrent and due to acute infection (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Parkinsonism due to human immunodeficiency virus infection (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Parkinsonism following infection (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Parkinsonism due to hereditary spastic paraplegia (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal.	Interprets	True	Movement	Inferred relationship	Some	3
Atypical Parkinsonism (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Parkinsonism due to heredodegenerative disorder (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment.	Interprets	True	Movement	Inferred relationship	Some	3
Infection causing parkinsonism (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Sporadic Parkinson disease (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Parkinsonism due to and following injury of head (disorder)	Interprets	True	Movement	Inferred relationship	Some	5
Parkinsonism due to mass lesion of brain (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Functional parkinsonism (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
A complex form of young-onset Parkinson disease that manifests with pyramidal signs, eye movement abnormalities, psychiatric manifestations (depression, anxiety, drug-induced psychosis, and impulse control disorders), intellectual disability, and other neurological symptoms (such as ataxia and epilepsy) along with classical parkinsonian symptoms.	Interprets	True	Movement	Inferred relationship	Some	3
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity.	Interprets	True	Movement	Inferred relationship	Some	3
A rare, genetic, parkinsonian disorder characterized by an age of onset between 21-45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints and falls, and other non-motor symptoms. A slow disease progression and a more pronounced response to dopaminergic therapy are also observed in most forms of this disease.	Interprets	True	Movement	Inferred relationship	Some	3
Parkinsonism with dementia of Guadeloupe is characterized by symmetrical bradykinesia, predominantly axial rigidity, postural instability with early falls and cognitive decline with prominent features of frontal lobe dysfunction.	Interprets	True	Movement	Inferred relationship	Some	4
A rare X-linked syndromic intellectual disability characterized by infantile-onset non-progressive intellectual deficit (with psychomotor developmental delay, cognitive impairment and macrocephaly) and early-onset parkinsonism (before 45 years of age), in male patients.	Interprets	True	Movement	Inferred relationship	Some	4
Hereditary late-onset Parkinson disease (LOPD) is a form of Parkinson disease (PD), characterized by an age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia (LID).	Interprets	True	Movement	Inferred relationship	Some	3
Infantile bilateral striatal necrosis (IBSN) comprises several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic.	Interprets	True	Movement	Inferred relationship	Some	3
Hemiparkinsonism-hemiatrophy syndrome is a rare parkinsonian disorder characterized by unilateral body atrophy and slowly progressive, ipsilateral, hemiparkinsonian signs (bradykinesia, rigidity, and tremor). Patients typically present with unilateral, action-induced dystonia, in upper or lower limbs, that progresses and becomes bilateral or with tremor which occurs predominantly at rest and progresses to hemiparkinsonism. Scoliosis, scapular winging, raised shoulders, brisk reflexes and extensor plantar responses are frequently associated.	Interprets	True	Movement	Inferred relationship	Some	4
A rare genetic neurological disorder with characteristics of the association of both parkinsonian (such as bradykinesia, rigidity and/or rest tremor) and pyramidal (such as increased reflexes, extensor plantar reflexes, pyramidal weakness or spasticity) manifestations, which vary according to the underlying associated disease (for example neurodegenerative disease, inborn errors of metabolism).	Interprets	True	Movement	Inferred relationship	Some	4
Sporadic infantile bilateral striatal necrosis	Interprets	True	Movement	Inferred relationship	Some	3
Autosomal recessive familial Parkinson disease	Interprets	True	Movement	Inferred relationship	Some	3
Progressive supranuclear palsy parkinsonism syndrome (disorder)	Interprets	True	Movement	Inferred relationship	Some	6
Neuroleptic-induced parkinsonism	Interprets	True	Movement	Inferred relationship	Some	3
Parkinson's disease	Interprets	True	Movement	Inferred relationship	Some	2
MPTP-induced parkinsonism	Interprets	True	Movement	Inferred relationship	Some	2
Parkinsonism caused by drug	Interprets	True	Movement	Inferred relationship	Some	2
Hemichorea	Interprets	True	Movement	Inferred relationship	Some	2
senil chorea	Interprets	False	Movement	Inferred relationship	Some	2
Juvenile cerebellar degeneration AND myoclonus	Interprets	True	Movement	Inferred relationship	Some	3
Atypical tic disorder	Interprets	True	Movement	Inferred relationship	Some	2
Extrapyramidal disease	Interprets	True	Movement	Inferred relationship	Some	2
Adductor spastic dysphonia of conversion reaction	Interprets	True	Movement	Inferred relationship	Some	5
Opticocochleodentate degeneration	Interprets	True	Movement	Inferred relationship	Some	2
Diffuse Lewy body disease	Interprets	True	Movement	Inferred relationship	Some	4
Hemiballism	Interprets	True	Movement	Inferred relationship	Some	2
Choreoacanthocytosis	Interprets	False	Movement	Inferred relationship	Some	2
Familial essential myoclonus	Interprets	True	Movement	Inferred relationship	Some	2
Olivopontocerebellar degeneration	Interprets	True	Movement	Inferred relationship	Some	2
Dentatorubropallidoluysian degeneration	Interprets	False	Movement	Inferred relationship	Some	2
Paradoxical facial movements	Interprets	False	Movement	Inferred relationship	Some	3
Chronic vocal tic disorder	Interprets	True	Movement	Inferred relationship	Some	3
Dyssynergia cerebellaris myoclonica	Interprets	True	Movement	Inferred relationship	Some	2
Spasmodic torticollis	Interprets	True	Movement	Inferred relationship	Some	3
Combined pyramidal-extrapyramidal syndrome (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
Paramyoclonus multiplex	Interprets	True	Movement	Inferred relationship	Some	3
Pallidonigroluysian degeneration	Interprets	True	Movement	Inferred relationship	Some	2
Electric chorea	Interprets	True	Movement	Inferred relationship	Some	2
Juvenile neuronal ceroid lipofuscinosis	Interprets	True	Movement	Inferred relationship	Some	2

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Id	Description	Lang	Type	Status	Case?	Module
380509014	Movement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
380510016	Quality of movement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2528848014	Movement (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2235911000005118	Bevægelse	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)