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363847004: 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
168701000077111 entité observable du mouvement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

345 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Movement observable Is a Neurological observable (observable entity) false Inferred relationship Some
Movement observable Is a Observable entity (observable entity) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Extension of left side of sacral spine Interprets True Movement observable Inferred relationship Some 3
Sporadic infantile bilateral striatal necrosis Interprets True Movement observable Inferred relationship Some 2
Injury to a joint due to an extension beyond the normal range of motion Interprets True Movement observable Inferred relationship Some 4
Injury to a joint due to flexion of a joint beyond its normal range of movement. Interprets True Movement observable Inferred relationship Some 4
Propriospinal myoclonus at sleep onset in infancy Interprets True Movement observable Inferred relationship Some 2
Hyperextension injury of finger (disorder) Interprets True Movement observable Inferred relationship Some 4
Hyperextension injury of thumb (disorder) Interprets True Movement observable Inferred relationship Some 4
Secondary parkinsonism Interprets True Movement observable Inferred relationship Some 2
Parkinsonism Interprets True Movement observable Inferred relationship Some 2
Spastic dysphonia Interprets True Movement observable Inferred relationship Some 3
Parkinson's disease Interprets True Movement observable Inferred relationship Some 2
Parkinsonism caused by drug Interprets True Movement observable Inferred relationship Some 2
Finding of movement of abdomen Interprets True Movement observable Inferred relationship Some 2
Carbon monoxide-induced parkinsonism Interprets True Movement observable Inferred relationship Some 2
Manganese-induced parkinsonism Interprets True Movement observable Inferred relationship Some 2
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 observable Inferred relationship Some 3
Parkinsonism with calcification of basal ganglia Interprets True Movement observable Inferred relationship Some 3
Postencephalitic parkinsonism Interprets True Movement observable Inferred relationship Some 3
Psychosis co-occurrent and due to Parkinson's disease (disorder) Interprets True Movement observable Inferred relationship Some 2
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 observable Inferred relationship Some 3
Bradykinesia (finding) Interprets True Movement observable Inferred relationship Some 1
Dissociative neurological symptom disorder co-occurrent with parkinsonism (disorder) Interprets True Movement observable Inferred relationship Some 2
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 observable Inferred relationship Some 3
On - off phenomenon (disorder) Interprets True Movement observable Inferred relationship Some 2
Functional parkinsonism (disorder) Interprets True Movement observable Inferred relationship Some 2
Neuroleptic-induced parkinsonism Interprets True Movement observable Inferred relationship Some 2
MPTP-induced parkinsonism Interprets True Movement observable Inferred relationship Some 2
Apraxia as late effect of cerebrovascular disease Interprets True Movement observable Inferred relationship Some 3
Ataxia due to disorder of immune function (disorder) Interprets True Movement observable Inferred relationship Some 2
Maternally-inherited mitochondrial dystonia is a rare neurological mitochondrial DNA-related disorder characterized clinically by progressive pediatric-onset dystonia with variable degrees of severity. Interprets True Movement observable Inferred relationship Some 2
A rare genetic neurodegenerative disease characterized by childhood onset of slowly progressive motor and cognitive regression, resulting in intellectual disability and loss of language and ambulation, associated with the appearance of dystonia, parkinsonism, chorea, or rigidity. Ataxia, dysarthria, and seizures have also been reported. Head circumference percentiles may decline over time. Brain imaging shows progressive cerebral and cerebellar atrophy, in some patients also thinning of the corpus callosum. Interprets True Movement observable Inferred relationship Some 4
A rare hyperkinetic movement disorder characterized by delayed motor development and infantile onset of axial hypotonia and a generalized hyperkinetic movement disorder, principally with dyskinesia of the limbs and trunk, and facial involvement including orolingual dyskinesia, drooling, and dysarthria. Variable hyperkinetic movements may include a jerky quality, intermittent chorea and ballismus. Brain imaging is normal and cognitive performance is typically preserved. Interprets True Movement observable Inferred relationship Some 2
A rare genetic neurodegenerative disease characterized by sudden onset of progressive motor deterioration and regression of developmental milestones. Manifestations include dystonia and muscle spasms, dysphagia, dysarthria, and eventually loss of speech and ambulation. Brain MRI shows predominantly striatal abnormalities. The disease is potentially associated with a fatal outcome. Interprets True Movement observable Inferred relationship Some 3
Finding of movement of shoulder (finding) Interprets True Movement observable Inferred relationship Some 2
Toxin-induced parkinsonism Interprets True Movement observable Inferred relationship Some 2
Parkinsonism caused by pesticide (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to Leigh syndrome Interprets True Movement observable Inferred relationship Some 2
Dopa responsive dystonia due to sepiapterin reductase deficiency (disorder) Interprets True Movement observable Inferred relationship Some 3
Callosity due to biting and/or chewing (disorder) Interprets True Movement observable Inferred relationship Some 4
Tic disorder due to rheumatic chorea Interprets True Movement observable Inferred relationship Some 3
Tic disorder due to prion disease Interprets True Movement observable Inferred relationship Some 3
A rare inborn error of metabolism characterized by increased serum phenylalanine, associated with variable neurological symptoms ranging from mild autistic features or hyperactivity to severe intellectual disability, dystonia, and parkinsonism. Laboratory analyses show normal tetrahydrobiopterin (BH4) metabolism and low levels of the CSF monoamine neurotransmitter metabolites homovanillic acid and 5-hydroxyindoleacetic acid. Interprets True Movement observable Inferred relationship Some 2
Habit tic affecting skin (disorder) Interprets True Movement observable Inferred relationship Some 3
Habit tic affecting hair (disorder) Interprets True Movement observable Inferred relationship Some 3
Tic disorder due to post-encephalitic syndrome Interprets True Movement observable Inferred relationship Some 3
Parkinsonism due to prion disease (disorder) Interprets True Movement observable Inferred relationship Some 3
Parkinsonism following Mycoplasma infection (disorder) Interprets True Movement observable Inferred relationship Some 2
Tic disorder due to encephalitis (disorder) Interprets True Movement observable Inferred relationship Some 3
Tic disorder due to neurosyphilis (disorder) Interprets True Movement observable Inferred relationship Some 3
Akathisia caused by drug (disorder) Interprets True Movement observable Inferred relationship Some 2
A rare neurologic disease characterized by the manifestation of an underlying psychiatric illness or malingering, and that cannot be attributed to any known structural or neurochemical diseases. Most cases fall in the psychiatric diagnostic category of conversion disorder, also referred to as functional neurological symptom disorder. Interprets True Movement observable Inferred relationship Some 1
Familial infantile bilateral striatal necrosis is the familial form of infantile bilateral striatal necrosis, a syndrome of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. Interprets True Movement observable Inferred relationship Some 2
A rare, genetic, neurological disorder characterized by childhood to adolescent onset of progressive myoclonus (which becomes very severe and results in major motor impediment) associated with infrequent tonic-clonic seizures, and, occasionally, ataxia. Learning disability prior to seizure onset and mild cognitive decline may be associated. Interprets True Movement observable Inferred relationship Some 3
Autoimmune generalized polymyoclonus Interprets True Movement observable Inferred relationship Some 2
Senile tremor Interprets True Movement observable Inferred relationship Some 1
A rare autosomal recessive cerebellar ataxia characterized by onset of dystonia and other extrapyramidal signs, ataxia, oculomotor apraxia, and progressive sensorimotor polyneuropathy in the first decade of life. Patients present distal muscle weakness and atrophy, decreased vibratory sensation, and areflexia, and usually become wheelchair-bound by the third decade. Variable cognitive impairment may also be seen. Interprets True Movement observable Inferred relationship Some 5
A rare genetic neurological disorder characterized by infantile hypotonia, congenital ophthalmic anomalies (including strabismus, esotropia, nystagmus, and central visual impairment), global developmental delay and intellectual disability, behavioral abnormalities, and movement disorder (such as dystonia, chorea, hyperkinesia, stereotypies). Mild facial dysmorphism and skeletal deformities have also been reported. EEG testing shows marked abnormalities in the absence of overt epileptic seizures. Interprets True Movement observable Inferred relationship Some 5
A rare mitochondrial oxidative phosphorylation disorder characterized by myoclonic seizures, ataxia, generalized epilepsy, muscle weakness and ragged red fibers in the muscle biopsy. Interprets True Movement observable Inferred relationship Some 4
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder) Interprets True Movement observable Inferred relationship Some 1
Autoimmune movement disorder Interprets True Movement observable Inferred relationship Some 1
Adult-onset familial idiopathic dystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
Adult-onset tic disorder (disorder) Interprets True Movement observable Inferred relationship Some 2
Adult-onset sporadic primary dystonia Interprets True Movement observable Inferred relationship Some 2
A rare genetic syndromic intellectual disability characterised by global developmental delay, moderate to severe intellectual disability, motor and language impairment, behavioural abnormalities (with mood instability, aggression, and self-mutilation), and progressive hand tremor. Facial dysmorphism includes narrow palpebral fissures, large ears, long philtrum, and prominent chin. Interprets True Movement observable Inferred relationship Some 5
Dissociative neurological symptom disorder with tremor (disorder) Interprets True Movement observable Inferred relationship Some 1
Dystonia due to Lesch Nyhan syndrome (disorder) Interprets True Movement observable Inferred relationship Some 3
Dystonia due to glutaric acidemia (disorder) Interprets True Movement observable Inferred relationship Some 3
Dystonia due to GM2 gangliosidosis Interprets True Movement observable Inferred relationship Some 3
Parkinsonism caused by dopamine receptor antagonist (disorder) Interprets True Movement observable Inferred relationship Some 2
Parkinsonism caused by dopamine depleting agent (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to hereditary disease (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to homocystinuria (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to hereditary spastic paraplegia (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to head injury (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to neutral 1 amino acid transport defect (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to encephalitis Interprets True Movement observable Inferred relationship Some 3
Dystonia due to familial basal ganglia calcifications Interprets True Movement observable Inferred relationship Some 2
Dystonia due to focal brain lesion Interprets True Movement observable Inferred relationship Some 3
Dystonia due to disorder of peripheral nervous system (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to cerebral anoxia Interprets True Movement observable Inferred relationship Some 2
Dystonia due to ataxia telangiectasia syndrome (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia caused by dopamine receptor antagonist (disorder) Interprets True Movement observable Inferred relationship Some 2
Dystonia due to Pelizaeus-Merzbacher disease (disorder) Interprets True Movement observable Inferred relationship Some 3
Dystonia due to mitochondrial disease (disorder) Interprets True Movement observable Inferred relationship Some 3
Dystonia due to Niemann-Pick disease type C (disorder) Interprets True Movement observable Inferred relationship Some 3
Dystonia due to Rett syndrome Interprets True Movement observable Inferred relationship Some 3
Dystonia due to perinatal cerebral injury (disorder) Interprets True Movement observable Inferred relationship Some 3
Dystonia due to metachromatic leucodystrophy (disorder) Interprets True Movement observable Inferred relationship Some 2
Jumpy stump syndrome (disorder) Interprets True Movement observable Inferred relationship Some 1
Dystonia due to Wilson disease (disorder) Interprets True Movement observable Inferred relationship Some 2
Myoclonic disorder due to sialidosis (disorder) Interprets True Movement observable Inferred relationship Some 2
Myoclonic disorder due to mitochondrial disorder (disorder) Interprets True Movement observable Inferred relationship Some 2
Myoclonic disorder due to hepatic failure (disorder) Interprets True Movement observable Inferred relationship Some 2
Myoclonic disorder due to neuronal ceroid lipofuscinosis (disorder) Interprets True Movement observable Inferred relationship Some 2
Familial multiple system tauopathy Interprets True Movement observable Inferred relationship Some 2
Myoclonic disorder due to dementia Interprets True Movement observable Inferred relationship Some 3
Myoclonic disorder due to uremia Interprets True Movement observable Inferred relationship Some 2
Hand tremor (finding) Interprets True Movement observable Inferred relationship Some 2
Lip tremor (finding) Interprets True Movement observable Inferred relationship Some 2
Postural tremor of upper limb (finding) Interprets True Movement observable Inferred relationship Some 2

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