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255324009: Movement (observable entity)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. Module: SNOMED CT core

    Descriptions:

    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
    42051000077112 mouvement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    mouvement Is a Gross motor functions (observable entity) false Inferred relationship Some
    mouvement Is a Process (observable entity) false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Extension of right side of sacral spine Interprets False mouvement Inferred relationship Some 3
    Extension of left side of sacral spine Interprets False mouvement Inferred relationship Some 3
    Bilateral sacral extension (finding) Interprets False mouvement Inferred relationship Some 3
    Flexion of left side of sacral spine (finding) Interprets False mouvement Inferred relationship Some 2
    Flexion of right side of sacral spine (finding) Interprets False mouvement Inferred relationship Some 2
    Bilateral sacral flexion (finding) Interprets False mouvement Inferred relationship Some 2
    Injury to a joint due to an extension beyond the normal range of motion Interprets False mouvement Inferred relationship Some 4
    Injury to a joint due to flexion of a joint beyond its normal range of movement. Interprets False mouvement Inferred relationship Some 4
    Propriospinal myoclonus at sleep onset in infancy Interprets False mouvement Inferred relationship Some 3
    Hyperextension injury of finger (disorder) Interprets False mouvement Inferred relationship Some 4
    Hyperextension injury of thumb (disorder) Interprets False mouvement Inferred relationship Some 4
    Hyperextension injury of neck Interprets False mouvement Inferred relationship Some 4
    Drug-induced dyskinesia Interprets False mouvement Inferred relationship Some 2
    Drug-induced dyskinesia, acute onset Interprets False mouvement Inferred relationship Some 3
    Tardive dyskinesia Interprets False mouvement Inferred relationship Some 2
    Neuroleptic-induced tardive dyskinesia Interprets False mouvement Inferred relationship Some 1
    Subacute dyskinesia caused by drug Interprets False mouvement Inferred relationship Some 1
    Paralysis of cervical sympathetic trunk (disorder) Interprets False mouvement Inferred relationship Some 3
    Acute mastoiditis with facial paralysis Interprets False mouvement Inferred relationship Some 4
    Rheumatic chorea with heart involvement Interprets False mouvement Inferred relationship Some 5
    Rheumatic chorea Interprets False mouvement Inferred relationship Some 5
    Rheumatic chorea without heart involvement Interprets False mouvement Inferred relationship Some 5
    Tremor due to pheochromocytoma Interprets False mouvement Inferred relationship Some 2
    Parkinsonism Interprets False mouvement 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 False mouvement Inferred relationship Some 4
    Bradykinesia (finding) Interprets False mouvement Inferred relationship Some 2
    Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder) Interprets False mouvement Inferred relationship Some 7
    Syphilitic parkinsonism Interprets False mouvement Inferred relationship Some 3
    Striatonigral degeneration Interprets False mouvement Inferred relationship Some 3
    Postencephalitic parkinsonism Interprets False mouvement Inferred relationship Some 4
    Juvenile Parkinson's disease Interprets False mouvement Inferred relationship Some 3
    Secondary parkinsonism Interprets False mouvement Inferred relationship Some 3
    Carbon monoxide-induced parkinsonism Interprets False mouvement Inferred relationship Some 4
    Manganese-induced parkinsonism Interprets False mouvement Inferred relationship Some 4
    Parkinsonism with calcification of basal ganglia Interprets False mouvement Inferred relationship Some 3
    Vascular parkinsonism Interprets False mouvement Inferred relationship Some 3
    Symptomatic parkinsonism Interprets False mouvement Inferred relationship Some 3
    On - off phenomenon (disorder) Interprets False mouvement Inferred relationship Some 4
    Impaired psychomotor performance (finding) Interprets False mouvement 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 False mouvement Inferred relationship Some 6
    Parkinsonism caused by carbon disulfide (disorder) Interprets False mouvement Inferred relationship Some 4
    Parkinsonism caused by methanol Interprets False mouvement Inferred relationship Some 4
    X-linked dystonia parkinsonism Interprets False mouvement Inferred relationship Some 3
    Perry syndrome Interprets False mouvement Inferred relationship Some 3
    Abrupt onset of dystonia with parkinsonism over a period of hours to days. Interprets False mouvement 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 False mouvement 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 False mouvement Inferred relationship Some 3
    Dissociative neurological symptom disorder co-occurrent with parkinsonism (disorder) Interprets False mouvement Inferred relationship Some 3
    A rare neuronal ceroid lipofuscinosis disorder characterized by juvenile-onset of 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 postmortem. Interprets False mouvement Inferred relationship Some 7
    Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder) Interprets False mouvement Inferred relationship Some 5
    Parkinsonism co-occurrent and due to acute infection (disorder) Interprets False mouvement Inferred relationship Some 4
    Parkinsonism due to human immunodeficiency virus infection (disorder) Interprets False mouvement Inferred relationship Some 3
    Parkinsonism following infection (disorder) Interprets False mouvement Inferred relationship Some 4
    Parkinsonism due to hereditary spastic paraplegia (disorder) Interprets False mouvement 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 False mouvement Inferred relationship Some 3
    Atypical Parkinsonism (disorder) Interprets False mouvement Inferred relationship Some 3
    Parkinsonism due to heredodegenerative disorder (disorder) Interprets False mouvement 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 False mouvement Inferred relationship Some 3
    Infection causing parkinsonism (disorder) Interprets False mouvement Inferred relationship Some 3
    Sporadic Parkinson disease (disorder) Interprets False mouvement Inferred relationship Some 3
    Parkinsonism due to and following injury of head (disorder) Interprets False mouvement Inferred relationship Some 5
    Parkinsonism due to mass lesion of brain (disorder) Interprets False mouvement Inferred relationship Some 4
    Functional parkinsonism (disorder) Interprets False mouvement 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 False mouvement Inferred relationship Some 3
    An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Interprets False mouvement 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 False mouvement 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 False mouvement 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 False mouvement 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 False mouvement 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 False mouvement 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 False mouvement Inferred relationship Some 4
    Parkinsonian-pyramidal syndrome is a rare, genetic, neurological disorder characterized by the association of both parkinsonian (i.e. bradykinesia, rigidity and/or rest tremor) and pyramidal (i.e. increased reflexes, extensor plantar reflexes, pyramidal weakness or spasticity) manifestations, which vary according to the underlying associated disease (e.g. neurodegenerative disease, inborn errors of metabolism). Interprets False mouvement Inferred relationship Some 4
    Sporadic infantile bilateral striatal necrosis Interprets False mouvement Inferred relationship Some 3
    Autosomal recessive familial Parkinson disease Interprets False mouvement Inferred relationship Some 3
    Progressive supranuclear palsy parkinsonism syndrome (disorder) Interprets False mouvement Inferred relationship Some 6
    Neuroleptic-induced parkinsonism Interprets False mouvement Inferred relationship Some 3
    Parkinson's disease Interprets False mouvement Inferred relationship Some 2
    MPTP-induced parkinsonism Interprets False mouvement Inferred relationship Some 2
    Parkinsonism caused by drug Interprets False mouvement Inferred relationship Some 2
    Hemichorea Interprets False mouvement Inferred relationship Some 2
    chorée de Bergeron Interprets False mouvement Inferred relationship Some 2
    Juvenile cerebellar degeneration AND myoclonus Interprets False mouvement Inferred relationship Some 3
    Atypical tic disorder Interprets False mouvement Inferred relationship Some 2
    Extrapyramidal disease Interprets False mouvement Inferred relationship Some 2
    Adductor spastic dysphonia of conversion reaction Interprets False mouvement Inferred relationship Some 5
    Opticocochleodentate degeneration Interprets False mouvement Inferred relationship Some 2
    Diffuse Lewy body disease (disorder) Interprets False mouvement Inferred relationship Some 4
    Hemiballism Interprets False mouvement Inferred relationship Some 2
    Choreoacanthocytosis Interprets False mouvement Inferred relationship Some 2
    Familial essential myoclonus Interprets False mouvement Inferred relationship Some 2
    Olivopontocerebellar degeneration Interprets False mouvement Inferred relationship Some 2
    Dentatorubropallidoluysian degeneration Interprets False mouvement Inferred relationship Some 2
    Paradoxical facial movements Interprets False mouvement Inferred relationship Some 3
    Chronic vocal tic disorder Interprets False mouvement Inferred relationship Some 3
    Dyssynergia cerebellaris myoclonica Interprets False mouvement Inferred relationship Some 2
    Spasmodic torticollis Interprets False mouvement Inferred relationship Some 3
    Combined pyramidal-extrapyramidal syndrome Interprets False mouvement Inferred relationship Some 2
    Paramyoclonus multiplex Interprets False mouvement Inferred relationship Some 3
    Pallidonigroluysian degeneration Interprets False mouvement Inferred relationship Some 2
    Electric chorea Interprets False mouvement Inferred relationship Some 2
    Juvenile neuronal ceroid lipofuscinosis Interprets False mouvement Inferred relationship Some 2

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