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255324009: Movement (observable entity)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2528848014 Movement (observable entity) en Fully specified name Active Case insensitive SNOMED CT core
380509014 Movement en Synonym Active Case insensitive SNOMED CT core
380510016 Quality of movement en Synonym Active Case insensitive SNOMED CT core

292 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Movement Is a Process true Inferred relationship Some
Movement Is a Gross motor functions false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Atypical juvenile parkinsonism Interprets True Movement Inferred relationship Some 3
Autosomal dominant striatal neurodegeneration Interprets True Movement Inferred relationship Some 3
Young onset Parkinson's disease Interprets True Movement Inferred relationship Some 3
Parkinsonism with dementia of Guadeloupe Interprets True Movement Inferred relationship Some 4
Early onset parkinsonism and intellectual disability syndrome Interprets True Movement Inferred relationship Some 4
Autosomal dominant late onset Parkinson disease Interprets True Movement Inferred relationship Some 3
Infantile striatonigral degeneration Interprets True Movement Inferred relationship Some 3
Hemiparkinsonism hemiatrophy syndrome Interprets True Movement Inferred relationship Some 4
Parkinsonian pyramidal syndrome Interprets True Movement Inferred relationship Some 4
Sporadic infantile bilateral striatal necrosis Interprets True Movement Inferred relationship Some 3
Autosomal recessive familial Parkinson disease Interprets True Movement Inferred relationship Some 3
Progressive supranuclear palsy parkinsonism syndrome Interprets True Movement Inferred relationship Some 6
Parkinsonism caused by neuroleptic drug Interprets True Movement Inferred relationship Some 3
Parkinson's disease Interprets True Movement Inferred relationship Some 2
MPTP-induced parkinsonism Interprets True Movement Inferred relationship Some 2
Parkinsonism due to drug Interprets True Movement Inferred relationship Some 2
Hemichorea Interprets True Movement Inferred relationship Some 2
Bergeron's chorea Interprets True Movement Inferred relationship Some 2
Juvenile cerebellar degeneration AND myoclonus Interprets True Movement Inferred relationship Some 3
Atypical tic disorder Interprets True Movement Inferred relationship Some 2
Extrapyramidal disease Interprets True Movement Inferred relationship Some 2
Adductor spastic dysphonia of conversion reaction Interprets True Movement Inferred relationship Some 5
Opticocochleodentate degeneration Interprets True Movement Inferred relationship Some 2
Diffuse Lewy body disease Interprets True Movement Inferred relationship Some 4
Hemiballism Interprets True Movement Inferred relationship Some 2
Choreoacanthocytosis Interprets True Movement Inferred relationship Some 2
Familial essential myoclonus Interprets True Movement Inferred relationship Some 2
Olivopontocerebellar degeneration Interprets True Movement Inferred relationship Some 2
Dentatorubropallidoluysian degeneration Interprets True Movement Inferred relationship Some 2
Paradoxical facial movements Interprets False Movement Inferred relationship Some 3
Chronic vocal tic disorder Interprets True Movement Inferred relationship Some 3
Dyssynergia cerebellaris myoclonica Interprets True Movement Inferred relationship Some 2
Spasmodic torticollis Interprets True Movement Inferred relationship Some 3
Combined pyramidal-extrapyramidal syndrome Interprets True Movement Inferred relationship Some 2
Paramyoclonus multiplex Interprets True Movement Inferred relationship Some 3
Pallidonigroluysian degeneration Interprets True Movement Inferred relationship Some 2
Electric chorea Interprets True Movement Inferred relationship Some 2
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
Henoch's chorea Interprets True Movement Inferred relationship Some 2
Pallidonigrospinal degeneration Interprets True Movement Inferred relationship Some 2
Tic of organic origin Interprets True Movement Inferred relationship Some 2
Symptomatic torsion dystonia Interprets True Movement Inferred relationship Some 2
Adductor spastic dysphonia of organic voice tremor Interprets True Movement Inferred relationship Some 3
Pallidonigral degeneration Interprets True 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 True 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
Neuroleptic-induced acute akathisia Interprets True Movement Inferred relationship Some 4
Dysphonia of Gilles de la Tourette's syndrome Interprets True Movement Inferred relationship Some 3
Myoclonic seizure Interprets False Movement Inferred relationship Some 2
Sialidosis 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
Medicine-induced postural tremor Interprets True Movement Inferred relationship Some 3
Progressive cerebellar tremor Interprets True Movement Inferred relationship Some 2
Pallidopontonigral degeneration Interprets True Movement Inferred relationship Some 2
Diffuse Lewy body disease with spongiform cortical change Interprets True Movement Inferred relationship Some 4
Choreoathetosis Interprets True Movement Inferred relationship Some 2
Juvenile paralysis agitans of Hunt Interprets True Movement Inferred relationship Some 2
Early myoclonic encephalopathy Interprets True 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 True Movement Inferred relationship Some 2
Neurologic adductor spastic dysphonia Interprets True Movement Inferred relationship Some 3
Orofacial dyskinesia Interprets True Movement Inferred relationship Some 2
Paroxysmal choreoathetosis Interprets True 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 True 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
Tourette's syndrome Interprets True Movement Inferred relationship Some 2
Stiff-man syndrome Interprets True Movement Inferred relationship Some 3
Athetosis with spastic paraplegia Interprets True Movement Inferred relationship Some 4
Juvenile myoclonic epilepsy 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 True 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 Interprets True Movement Inferred relationship Some 2
Hypotonic cerebral palsy Interprets True Movement Inferred relationship Some 4

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Reference Sets

Observable entity foundation reference set

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