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

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
Choreoathetosis	Interprets	False	mouvement	Inferred relationship	Some	3
Chorea due to inherited organic acidemia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to and following injury of head (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Chorea due to antiphospholipid syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to chronic hepatocerebral degeneration	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to endocrine disorder	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to hyperglycemia	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to tardive dyskinesia	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to prion disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to Lesch-Nyhan syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to metabolic disorder	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to inherited aminoaciduria (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to anoxia of brain (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea caused by dopamine receptor antagonist (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to hereditary ataxia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to and following ventriculoperitoneal shunt (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Chorea caused by oral contraceptive (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to cerebral injury due to birth trauma (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to ataxia telangiectasia syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to immunological disorder (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to neuroferritinopathy	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to polycythemia rubra vera	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to widespread metastatic malignant neoplastic disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to hypoparathyroidism (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to classical pantothenate kinase associated neurodegeneration (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to mitochondrial cytopathy	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to inborn error of metabolism (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to paraneoplastic syndrome	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to hyponatremia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Choreoacanthocytosis	Interprets	False	mouvement	Inferred relationship	Some	3
Dentatorubropallidoluysian degeneration	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea due to immunoglobulin A vasculitis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Wilson's disease	Interprets	False	mouvement	Inferred relationship	Some	6
Pallidonigrospinal degeneration	Interprets	False	mouvement	Inferred relationship	Some	3
Rheumatic chorea with heart involvement	Interprets	False	mouvement	Inferred relationship	Some	8
Huntington's chorea	Interprets	False	mouvement	Inferred relationship	Some	7
Pallidonigral degeneration	Interprets	False	mouvement	Inferred relationship	Some	3
Dubini's chorea	Interprets	False	mouvement	Inferred relationship	Some	3
Pallidopontonigral degeneration	Interprets	False	mouvement	Inferred relationship	Some	3
Juvenile paralysis agitans of Hunt	Interprets	False	mouvement	Inferred relationship	Some	3
Birnbaum's syndrome	Interprets	False	mouvement	Inferred relationship	Some	4
Rheumatic chorea	Interprets	False	mouvement	Inferred relationship	Some	8
Pallidoluysian degeneration	Interprets	False	mouvement	Inferred relationship	Some	3
Pigmentary pallidal degeneration	Interprets	False	mouvement	Inferred relationship	Some	3
Rheumatic chorea without heart involvement	Interprets	False	mouvement	Inferred relationship	Some	8
Juvenile onset Huntington's disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	7
Late onset Huntington's disease	Interprets	False	mouvement	Inferred relationship	Some	7
Akinetic-rigid form of Huntington's disease	Interprets	False	mouvement	Inferred relationship	Some	7
Pallidal degeneration	Interprets	False	mouvement	Inferred relationship	Some	3
Benign hereditary chorea	Interprets	False	mouvement	Inferred relationship	Some	3
Chorea due to systemic lupus erythematosus (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Chorea due to thyrotoxicosis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Kinesiogenic choreoathetosis	Interprets	False	mouvement	Inferred relationship	Some	3
Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another.	Interprets	False	mouvement	Inferred relationship	Some	3
Toxic chorea (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Paroxysmal nonkinesigenic dyskinesia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Paroxysmal kinesigenic dyskinesia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Huntington disease-like syndrome	Interprets	False	mouvement	Inferred relationship	Some	3
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	False	mouvement	Inferred relationship	Some	4
Dissociative neurological symptom disorder co-occurrent with chorea	Interprets	False	mouvement	Inferred relationship	Some	3
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	False	mouvement	Inferred relationship	Some	3
Infection causing chorea (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Chorea due to and following infective disorder (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Chorea co-occurrent and due to dentatorubropallidoluysian degeneration (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
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	False	mouvement	Inferred relationship	Some	5
Acquired choreiform dyspraxia	Interprets	False	mouvement	Inferred relationship	Some	7
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	False	mouvement	Inferred relationship	Some	3
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	False	mouvement	Inferred relationship	Some	3
Chorea due to and following encephalitis	Interprets	False	mouvement	Inferred relationship	Some	5
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	False	mouvement	Inferred relationship	Some	3
Classical pantothenate kinase associated neurodegeneration	Interprets	False	mouvement	Inferred relationship	Some	3
Atypical pantothenate kinase associated neurodegeneration (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
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	False	mouvement	Inferred relationship	Some	13
Post-hemiplegic chorea	Interprets	False	mouvement	Inferred relationship	Some	4
Acquired ataxia due to vitamin deficiency	Interprets	False	mouvement	Inferred relationship	Some	2
Andersen Tawil syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Astasia-abasia	Interprets	False	mouvement	Inferred relationship	Some	1
Dissociative paralysis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Dissociative astasia-abasia	Interprets	False	mouvement	Inferred relationship	Some	1
Dissociative motor disorder	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to injury of head (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea following injury	Interprets	False	mouvement	Inferred relationship	Some	4
A rare persistent combined dystonia characterized by childhood onset of progressive dystonia typically beginning in the lower limbs and eventually progressing to generalized dystonia with involvement of the upper limbs, trunk, face, and neck. Variable developmental delay and intellectual disability, as well as mild microcephaly, short stature, abnormal eye movements, and slightly dysmorphic facial features have been reported in association.	Interprets	False	mouvement	Inferred relationship	Some	3
Fisher's syndrome	Interprets	False	mouvement	Inferred relationship	Some	6
Dissociative neurological symptom disorder co-occurrent with facial spasm	Interprets	False	mouvement	Inferred relationship	Some	3
Dissociative neurological disorder with symptom of movement disorder (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Dissociative astasia-abasia	Interprets	False	mouvement	Inferred relationship	Some	3
Astasia-abasia	Interprets	False	mouvement	Inferred relationship	Some	3
Movement of eyelid	Is a	False	mouvement	Inferred relationship	Some
Lacunar ataxic hemiparesis	Interprets	False	mouvement	Inferred relationship	Some	4
Lacunar ataxic hemiparesis of right dominant side	Interprets	False	mouvement	Inferred relationship	Some	7
Lacunar ataxic hemiparesis of left dominant side	Interprets	False	mouvement	Inferred relationship	Some	7
Lacunar ataxic hemiparesis of left nondominant side	Interprets	False	mouvement	Inferred relationship	Some	7
Lacunar ataxic hemiparesis of right nondominant side	Interprets	False	mouvement	Inferred relationship	Some	7
Pure motor lacunar infarction	Interprets	False	mouvement	Inferred relationship	Some	5
Pure sensorimotor lacunar infarction	Interprets	False	mouvement	Inferred relationship	Some	5
Dysarthria-clumsy hand syndrome	Interprets	False	mouvement	Inferred relationship	Some	3
A rare genetic neurological disorder with characteristics of childhood onset of severe global neurodevelopmental regression with eventual loss of independent walking and loss of language and fine and gross motor skills, and development of severe dysphagia requiring tube feeding, seizures, cerebellar syndrome, dystonia, and other neurologic manifestations. Brain imaging shows progressive cerebral and/or cerebellar atrophy in most cases. A less severe phenotype associated with missense mutations shows no regression or movement abnormalities, ambulation is preserved, and brain imaging is normal.	Interprets	False	mouvement	Inferred relationship	Some	4
Facial palsy House-Brackmann grade V of right facial nerve (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Facial palsy House-Brackmann grade V of left facial nerve (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Facial palsy House-Brackmann grade VI of left facial nerve (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3

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