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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
Pallidonigral degeneration Interprets True Movement observable Inferred relationship Some 2
Dubini's chorea Interprets True Movement observable Inferred relationship Some 2
Pallidopontonigral degeneration Interprets True Movement observable Inferred relationship Some 2
Juvenile paralysis agitans of Hunt Interprets True Movement observable Inferred relationship Some 2
Chorea gravidarum Interprets True Movement observable Inferred relationship Some 4
Birnbaum's syndrome Interprets True Movement observable Inferred relationship Some 2
Rheumatic chorea Interprets True Movement observable Inferred relationship Some 5
Pallidoluysian degeneration Interprets True Movement observable Inferred relationship Some 2
Pigmentary pallidal degeneration Interprets True Movement observable Inferred relationship Some 2
Chronic progressive non-hereditary chorea Interprets True Movement observable Inferred relationship Some 4
Rheumatic chorea without heart involvement Interprets True Movement observable Inferred relationship Some 5
Westphal-Strumpell syndrome Interprets True Movement observable Inferred relationship Some 6
Juvenile onset Huntington's disease (disorder) Interprets True Movement observable Inferred relationship Some 1
Late onset Huntington's disease Interprets True Movement observable Inferred relationship Some 1
Akinetic-rigid form of Huntington's disease Interprets True Movement observable Inferred relationship Some 1
Pallidal degeneration Interprets True Movement observable Inferred relationship Some 2
Benign hereditary chorea Interprets True Movement observable Inferred relationship Some 2
Chorea due to systemic lupus erythematosus (disorder) Interprets True Movement observable Inferred relationship Some 2
Chorea due to thyrotoxicosis (disorder) Interprets True Movement observable Inferred relationship Some 2
Kinesiogenic choreoathetosis Interprets True Movement observable 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 Inferred relationship Some 1
Toxic chorea (disorder) Interprets True Movement observable Inferred relationship Some 2
Paroxysmal nonkinesigenic dyskinesia (disorder) Interprets True Movement observable Inferred relationship Some 3
Paroxysmal kinesigenic dyskinesia (disorder) Interprets True Movement observable Inferred relationship Some 3
Choreic cerebral palsy Interprets True Movement observable 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 Inferred relationship Some 2
Huntington disease-like syndrome Interprets True Movement observable 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 Inferred relationship Some 3
Dissociative neurological symptom disorder co-occurrent with chorea Interprets True Movement observable 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 Inferred relationship Some 2
Infection causing chorea (disorder) Interprets True Movement observable Inferred relationship Some 2
Chorea due to and following infective disorder (disorder) Interprets True Movement observable Inferred relationship Some 4
Chorea co-occurrent and due to dentatorubropallidoluysian degeneration (disorder) Interprets True Movement observable 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 Inferred relationship Some 4
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder) Interprets True Movement observable Inferred relationship Some 2
Acquired choreiform dyspraxia Interprets True Movement observable Inferred relationship Some 6
A rare, genetic neurodegenerative disease characterized by movement disorders, including dystonia, chorea, myoclonus, tremor and rigidity. Associated features are also cognitive and memory impairment, early psychiatric disturbances and behavioral problems. Interprets True Movement observable Inferred relationship Some 2
A rare, genetic, human prion disease characterized by adult-onset neurodegenerative manifestations associated with a movement disorder and psychiatric/behavioral 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 generalized spasticity, seizures, urine incontinence and pyramidal abnormalities. Interprets True Movement observable Inferred relationship Some 2
Chorea due to and following encephalitis Interprets True Movement observable 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 Inferred relationship Some 2
Classical pantothenate kinase associated neurodegeneration Interprets True Movement observable Inferred relationship Some 2
Atypical pantothenate kinase associated neurodegeneration (disorder) Interprets True Movement observable 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 Inferred relationship Some 8
Hemichorea Interprets True Movement observable Inferred relationship Some 3
Post-hemiplegic chorea Interprets True Movement observable Inferred relationship Some 1
Hemichorea due to injury of head (disorder) Interprets True Movement observable Inferred relationship Some 4
Hemichorea due to cerebral arteriovenous malformation (disorder) Interprets True Movement observable Inferred relationship Some 4
Hemichorea due to abscess of brain (disorder) Interprets True Movement observable Inferred relationship Some 4
Hemichorea due to cerebral hemorrhage (disorder) Interprets True Movement observable Inferred relationship Some 4
Hemichorea due to neoplasm of brain (disorder) Interprets True Movement observable Inferred relationship Some 4
Hemichorea due to cerebral infarction (disorder) Interprets True Movement observable Inferred relationship Some 4
Hemichorea due to multiple sclerosis (disorder) Interprets True Movement observable Inferred relationship Some 1
Andersen Tawil syndrome (disorder) Interprets True Movement observable Inferred relationship Some 1
Chorea due to injury of head (disorder) Interprets True Movement observable Inferred relationship Some 1
Chorea following injury Interprets True Movement observable Inferred relationship Some 1
Movement of foot Is a True Movement observable Inferred relationship Some
Fisher's syndrome Interprets True Movement observable Inferred relationship Some 5
Lacunar ataxic hemiparesis Interprets True Movement observable Inferred relationship Some 1
Lacunar ataxic hemiparesis of right dominant side Interprets True Movement observable Inferred relationship Some 5
Lacunar ataxic hemiparesis of left dominant side Interprets True Movement observable Inferred relationship Some 5
Lacunar ataxic hemiparesis of left nondominant side Interprets True Movement observable Inferred relationship Some 5
Lacunar ataxic hemiparesis of right nondominant side Interprets True Movement observable Inferred relationship Some 5
Pure motor lacunar infarction Interprets True Movement observable Inferred relationship Some 1
Pure sensorimotor lacunar infarction Interprets True Movement observable Inferred relationship Some 7
Facial palsy House-Brackmann grade V of right facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Facial palsy House-Brackmann grade V of left facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Facial palsy House-Brackmann grade VI of left facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Facial palsy House-Brackmann grade VI of right facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Facial palsy House-Brackmann grade IV of left facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Right facial palsy House-Brackmann grade IV Interprets True Movement observable Inferred relationship Some 2
Left facial palsy House-Brackmann grade III Interprets True Movement observable Inferred relationship Some 2
Facial palsy House-Brackmann grade III of right facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Facial palsy House-Brackmann grade II of left facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Facial palsy House-Brackmann grade II of right facial nerve (disorder) Interprets True Movement observable Inferred relationship Some 2
Progressive external ophthalmoplegia of left eye (disorder) Interprets True Movement observable Inferred relationship Some 3
Right progressive external ophthalmoplegia Interprets True Movement observable Inferred relationship Some 3
Tolosa-Hunt syndrome of left eye Interprets True Movement observable Inferred relationship Some 2
Tolosa-Hunt syndrome of right eye (disorder) Interprets True Movement observable Inferred relationship Some 2
Tolosa-Hunt syndrome of bilateral eyes (disorder) Interprets True Movement observable Inferred relationship Some 3
A rare disorder of fatty acid biosynthesis characterised by spastic paraparesis, bilateral congenital/juvenile cataracts, gross motor developmental delay, speech delay and truncal hypotonia. Seizures in infancy can also be observed. Patients have elevated levels of ether lipids including plasmalogen. Majority of the affected individuals have normal brain imaging and normal growth. No microcephaly or dysmorphic features were reported. Interprets True Movement observable Inferred relationship Some 9
Dystonic tremor (finding) Interprets True Movement observable Inferred relationship Some 1
Myoclonus associated with fever Interprets True Movement observable Inferred relationship Some 3
Psychogenic dyskinesia Interprets True Movement observable Inferred relationship Some 1
Myoclonic dystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
Nuchal rigidity (finding) Interprets True Movement observable Inferred relationship Some 2
Nuchal rigidity due to meningitis (finding) Interprets True Movement observable Inferred relationship Some 3
Nuchal rigidity due to subarachnoid hemorrhage (finding) Interprets True Movement observable Inferred relationship Some 3
Generalized dystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
Physiological tremor (finding) Interprets True Movement observable Inferred relationship Some 1
Myoclonus of stapedius muscle (disorder) Interprets True Movement observable Inferred relationship Some 3
Ballism (disorder) Interprets True Movement observable Inferred relationship Some 2
Non-epileptic myoclonus (disorder) Interprets True Movement observable Inferred relationship Some 2
Hemidystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
Compensated movement at site of pain (finding) Interprets True Movement observable Inferred relationship Some 1
Reflex blepharospasm (disorder) Interprets True Movement observable Inferred relationship Some 4
Involuntary truncal rocking (finding) Interprets True Movement observable Inferred relationship Some 1
Post-anoxic myoclonus Interprets True Movement observable Inferred relationship Some 3
Attacks of floppiness Interprets True Movement observable Inferred relationship Some 1
Attacks of rigidity Interprets True Movement observable Inferred relationship Some 1
Flinging movement Interprets True Movement observable Inferred relationship Some 2
constatation concernant la réponse motrice Interprets True Movement observable Inferred relationship Some 1

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