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
Juvenile neuronal ceroid lipofuscinosis	Interprets	True	Movement	Inferred relationship	Some	2
Spastic pseudobulbar dysphonia	Interprets	True	Movement	Inferred relationship	Some	3
Mixed flaccid-spastic pseudobulbar dysphonia	Interprets	True	Movement	Inferred relationship	Some	3
Chorea due to immunoglobulin A vasculitis (disorder)	Interprets	False	Movement	Inferred relationship	Some	2
Pallidonigrospinal degeneration	Interprets	False	Movement	Inferred relationship	Some	2
Tic of organic origin (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
Symptomgivende torsionsdystoni	Interprets	False	Movement	Inferred relationship	Some	2
Adductor spastic dysphonia of organic voice tremor	Interprets	True	Movement	Inferred relationship	Some	3
Pallidonigral degeneration	Interprets	False	Movement	Inferred relationship	Some	2
Adductor spastic dysphonia of dystonia	Interprets	True	Movement	Inferred relationship	Some	3
Dysmorphic sialidosis with renal involvement	Interprets	True	Movement	Inferred relationship	Some	4
Dubini's chorea	Interprets	False	Movement	Inferred relationship	Some	2
Neuroleptic-induced acute dystonia	Interprets	True	Movement	Inferred relationship	Some	4
Adductor spastic dysphonia of musculoskeletal tension reaction	Interprets	True	Movement	Inferred relationship	Some	3
Dysmorphic sialidosis, infantile form	Interprets	True	Movement	Inferred relationship	Some	4
Organic writer's cramp	Interprets	True	Movement	Inferred relationship	Some	2
Dysmorphic sialidosis	Interprets	True	Movement	Inferred relationship	Some	3
Dystonia lenticularis	Interprets	True	Movement	Inferred relationship	Some	2
Posthemiplegic athetosis	Interprets	True	Movement	Inferred relationship	Some	2
Acute akathisia caused by neuroleptic (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Dysphonia of Gilles de la Tourette's syndrome	Interprets	True	Movement	Inferred relationship	Some	3
Myoklonusanfald	Interprets	False	Movement	Inferred relationship	Some	2
A lysosomal storage disease, belonging to the group of oligosaccharidosis or with a wide clinical spectrum that is divided into two main clinical subtypes: sialidosis type I, the milder, non dysmorphic form of the disease with characteristics of gait abnormalities, progressive visual loss, bilateral macular cherry red spots and myoclonus, that presents in adolescence or adulthood (second or third decade of life); and sialidosis type II (see this term) the more severe, early onset form, with characteristics of progressive and severe mucopolysaccharidosis-like phenotype with coarse facies, visceromegaly, dysostosis multiplex, and developmental delay. Bilateral macular cherry red spots are also present. Sialidosis type II has been further divided into congenital (with hydrops fetalis), infantile and juvenile presentations.	Interprets	True	Movement	Inferred relationship	Some	3
Grimaces	Interprets	True	Movement	Inferred relationship	Some	2
Dysphonia of palatopharyngolaryngeal myoclonus	Interprets	True	Movement	Inferred relationship	Some	6
Abductor spastic dysphonia	Interprets	True	Movement	Inferred relationship	Some	3
Medication-induced postural tremor	Interprets	True	Movement	Inferred relationship	Some	3
Progressive cerebellar tremor	Interprets	True	Movement	Inferred relationship	Some	2
Pallidopontonigral degeneration	Interprets	False	Movement	Inferred relationship	Some	2
Diffuse Lewy body disease with spongiform cortical change	Interprets	True	Movement	Inferred relationship	Some	4
Choreoathetosis	Interprets	False	Movement	Inferred relationship	Some	2
Juvenile paralysis agitans of Hunt	Interprets	False	Movement	Inferred relationship	Some	2
Early myoclonic encephalopathy	Interprets	False	Movement	Inferred relationship	Some	2
Athetosis	Interprets	True	Movement	Inferred relationship	Some	2
Psychogenic adductor spastic dysphonia	Interprets	True	Movement	Inferred relationship	Some	4
Dysmorphic sialidosis, congenital form	Interprets	True	Movement	Inferred relationship	Some	2
Spastic dysphonia	Interprets	True	Movement	Inferred relationship	Some	3
Idiopathic adductor spastic dysphonia	Interprets	True	Movement	Inferred relationship	Some	3
Birnbaum's syndrome	Interprets	False	Movement	Inferred relationship	Some	2
Neurologic adductor spastic dysphonia	Interprets	True	Movement	Inferred relationship	Some	3
Orofacial dyskinesia (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
Paroxysmal choreoathetosis	Interprets	False	Movement	Inferred relationship	Some	3
Neuroleptic malignant syndrome	Interprets	True	Movement	Inferred relationship	Some	3
Dystonia	Interprets	True	Movement	Inferred relationship	Some	2
Corticobasal degeneration	Interprets	True	Movement	Inferred relationship	Some	3
Pallidoluysian degeneration	Interprets	False	Movement	Inferred relationship	Some	2
Athetosis with rigidity	Interprets	True	Movement	Inferred relationship	Some	2
Adductor spastic dysphonia	Interprets	True	Movement	Inferred relationship	Some	3
Gilles de la Tourette's syndrome	Interprets	True	Movement	Inferred relationship	Some	2
A rare neurological disorder comprising fluctuating trunk and limb stiffness, painful muscle spasms, task-specific phobia, an exaggerated startle response, and ankylosing deformities such as fixed lumbar hyperlordosis. Age of onset peaks around 45 and symptoms develop over months or years. Progressive muscle stiffness renders the trunk and hips immobile and the gait becomes stiff and awkward. The presence of antibodies against glutamic acid decarboxylase (GAD-Abs) in more than 70% of cases suggests an autoimmune pathogenesis. GAD-Abs may block synthesis of the inhibitory neurotransmitter, gamma-aminobutyric acid (GABA) thereby attenuating inhibition of spinal motoneurones.	Interprets	True	Movement	Inferred relationship	Some	3
Athetosis with spastic paraplegia	Interprets	True	Movement	Inferred relationship	Some	4
A type of epilepsy that presents with myoclonic epileptic seizures, usually between 10 and 24 years of age, in an otherwise normal adolescent or adult. Generalized tonic-clonic seizures occur in greater than 90 percent of individuals and absence seizures occur in a third. Seizures typically occur shortly after waking and when tired. Sleep deprivation is an important provoking factor. Photosensitivity is common. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalized spike-wave and polyspike-wave and a normal background.	Interprets	False	Movement	Inferred relationship	Some	2
Chronic motor tic disorder	Interprets	True	Movement	Inferred relationship	Some	3
Transient tic disorder, single episode	Interprets	True	Movement	Inferred relationship	Some	3
Palatal myoclonus	Interprets	True	Movement	Inferred relationship	Some	4
Tic disorder	Interprets	True	Movement	Inferred relationship	Some	2
Pigmentary pallidal degeneration	Interprets	False	Movement	Inferred relationship	Some	2
Chronic progressive non-hereditary chorea	Interprets	True	Movement	Inferred relationship	Some	3
Dysmorphic sialidosis, juvenile form	Interprets	True	Movement	Inferred relationship	Some	4
Myoclonic disorder	Interprets	True	Movement	Inferred relationship	Some	2
Progressive pyramidopallidal degeneration	Interprets	True	Movement	Inferred relationship	Some	2
Transient childhood tic	Interprets	True	Movement	Inferred relationship	Some	4
Fragments of torsion dystonia (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
A form of non-spastic cerebral palsy with decreased muscle tone, noticeably floppy muscles with poor or no head control.	Interprets	True	Movement	Inferred relationship	Some	4
Mirror movements	Interprets	True	Movement	Inferred relationship	Some	2
Oral dystonia	Interprets	True	Movement	Inferred relationship	Some	3
Oral dyskinesia	Interprets	False	Movement	Inferred relationship	Some	3
Olivopontocerebellar atrophy with slow eye movement	Interprets	True	Movement	Inferred relationship	Some	2
Olivopontocerebellar atrophy with blindness	Interprets	True	Movement	Inferred relationship	Some	2
Kinesiogenic choreoathetosis	Interprets	False	Movement	Inferred relationship	Some	2
Paroxysmal dystonia	Interprets	True	Movement	Inferred relationship	Some	3
A paroxysmal dystonic movement disorder occurring in association with gastro-oesophageal reflux, and, in some cases, hiatal hernia. The prevalence is unknown. Onset usually occurs during infancy or early childhood. The dystonic movements are characterised by abnormal posturing of the head and neck (torticollis) and severe arching of the spine. The dystonic movements are clearly associated with gastro-oesophageal reflux but the pathophysiological mechanism is not clearly understood.	Interprets	True	Movement	Inferred relationship	Some	5
Drug-induced acute dystonia	Interprets	True	Movement	Inferred relationship	Some	3
Drug-induced tardive dystonia	Interprets	True	Movement	Inferred relationship	Some	3
Idiopathic non-familial dystonia	Interprets	True	Movement	Inferred relationship	Some	2
Isolated cervical dystonia	Interprets	True	Movement	Inferred relationship	Some	2
Spasmodic retrocollis	Interprets	True	Movement	Inferred relationship	Some	2
Isolated blepharospasm	Interprets	True	Movement	Inferred relationship	Some	3
Meige syndrome	Interprets	True	Movement	Inferred relationship	Some	2
Isolated oromandibular dystonia	Interprets	True	Movement	Inferred relationship	Some	3
Posthemiplegic dystonia	Interprets	True	Movement	Inferred relationship	Some	2
Occupational dystonia	Interprets	True	Movement	Inferred relationship	Some	2
Diurnal dystonia	Interprets	True	Movement	Inferred relationship	Some	2
Facial tic disorder	Interprets	True	Movement	Inferred relationship	Some	3
Vocal tic disorder	Interprets	True	Movement	Inferred relationship	Some	2
Motor tic disorder	Interprets	True	Movement	Inferred relationship	Some	2
Gestural tic disorder	Interprets	True	Movement	Inferred relationship	Some	3
symptomgivende myoklonus	Interprets	False	Movement	Inferred relationship	Some	2
Postencephalitic myoclonus	Interprets	True	Movement	Inferred relationship	Some	2
Drug-induced myoclonus	Interprets	True	Movement	Inferred relationship	Some	3
Segmental cord myoclonus	Interprets	True	Movement	Inferred relationship	Some	2
Palatal-tympanic myoclonus	Interprets	True	Movement	Inferred relationship	Some	2
Hyoid myoclonus	Interprets	True	Movement	Inferred relationship	Some	2
Opsoclonus-myoclonus syndrome	Interprets	True	Movement	Inferred relationship	Some	2
A type of epilepsy that presents with myoclonic-atonic seizures usually between 2 to 6 years of age. Other generalised seizure types which may be seen in this syndrome include atonic, myoclonic, generalised tonic-clonic seizures, tonic and absence seizures. Nonconvulsive status epilepticus is common. Development prior to seizure onset is normal in two thirds of cases. These children typically show developmental stagnation or even regression during the active seizures (stormy) phase, which improves once seizures are controlled. The electroencephalogram shows generalised 2 to 6 Hz spike-wave or polyspike-and-wave abnormalities, with normal background.	Interprets	False	Movement	Inferred relationship	Some	2
Unverricht-Lundborg syndrome	Interprets	False	Movement	Inferred relationship	Some	2
Lafora disease	Interprets	False	Movement	Inferred relationship	Some	2
A mitochondrial encephalomyopathy with characteristics of myoclonic seizures. Patients usually present during adolescence or early adulthood with myoclonic epilepsy, sometimes with neurosensory deafness, optic atrophy, short stature or peripheral neuropathy. The disease is progressive with worsening of the epilepsy and onset of additional symptoms including ataxia, deafness, muscle weakness, and dementia. Caused by mutations in the mitochondrial DNA.	Interprets	True	Movement	Inferred relationship	Some	4
Sleep-related dystonia	Interprets	True	Movement	Inferred relationship	Some	2
Cluster tic syndrome	Interprets	True	Movement	Inferred relationship	Some	2
Painful legs and moving toes	Interprets	True	Movement	Inferred relationship	Some	4

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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)