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255324009: Movement (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
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

327 descendants. Search Descendants:

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
Painful legs and moving toes Interprets True Movement Inferred relationship Some 4
Progressive myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
Senile dementia of the Lewy body type Interprets True Movement Inferred relationship Some 5
Autosomal dominant idiopathic familial dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Tic caused by drug Interprets True Movement Inferred relationship Some 3
Post-anoxic myoclonus Interprets True Movement Inferred relationship Some 3
Generalized dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Myoclonus of stapedius muscle (disorder) Interprets True Movement Inferred relationship Some 3
Non-epileptic myoclonus (disorder) Interprets True Movement Inferred relationship Some 2
Hemidystonia (disorder) Interprets True Movement Inferred relationship Some 2
Reflex blepharospasm (disorder) Interprets True Movement Inferred relationship Some 4
Severe myoclonic epilepsy in infancy Interprets False Movement Inferred relationship Some 2
Myoclonus associated with fever Interprets True Movement Inferred relationship Some 3
Myoclonic dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Habit tic (disorder) Interprets True Movement Inferred relationship Some 3
Habit tic affecting skin (disorder) Interprets True Movement Inferred relationship Some 3
Habit tic affecting hair (disorder) Interprets True Movement Inferred relationship Some 3
Recurrent transient tic disorder Interprets True Movement Inferred relationship Some 4
Medication-induced movement disorder Interprets True Movement Inferred relationship Some 3
Drug-induced dystonia Interprets True Movement Inferred relationship Some 3
Drug-induced orofacial dyskinesia Interprets True Movement Inferred relationship Some 3
Benign neonatal sleep myoclonus (disorder) Interprets True Movement Inferred relationship Some 3
Transient tic disorder Interprets True Movement Inferred relationship Some 3
Myoclonus of tensor tympani muscle (disorder) Interprets True Movement Inferred relationship Some 3
Segmental dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Torsion dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Autoimmune opsoclonus myoclonus Interprets True Movement Inferred relationship Some 3
Acquired ataxia Interprets True Movement Inferred relationship Some 2
Ataxia due to chronic infection of central nervous system (disorder) Interprets True Movement Inferred relationship Some 3
Toxic dystonia Interprets True Movement Inferred relationship Some 2
Paroxysmal nonkinesigenic dyskinesia (disorder) Interprets False Movement Inferred relationship Some 3
Paroxysmal kinesigenic dyskinesia (disorder) Interprets False Movement Inferred relationship Some 3
Essential tremor Interprets True Movement Inferred relationship Some 2
Laryngeal dystonia Interprets True Movement Inferred relationship Some 3
Nocturnal myoclonus Interprets False Movement Inferred relationship Some 2
Organic sleep related movement disorder (disorder) Interprets True Movement Inferred relationship Some 2
Brainstem myoclonus Interprets True Movement Inferred relationship Some 2
Refractory juvenile myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
Cerebral cortex myoclonus (disorder) Interprets True Movement Inferred relationship Some 2
Spinal cord myoclonus Interprets True Movement Inferred relationship Some 2
Autosomal recessive idiopathic familial dystonia Interprets True Movement Inferred relationship Some 2
Ataxic cerebral palsy Interprets True Movement Inferred relationship Some 4
Congenital athetosis Interprets True Movement Inferred relationship Some 2
Non-spastic cerebral palsy (disorder) Interprets True Movement Inferred relationship Some 4
Progressive myoclonus epilepsy with ataxia (disorder) Interprets False Movement Inferred relationship Some 2
Huntington disease-like syndrome Interprets False Movement Inferred relationship Some 2
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis Interprets True Movement Inferred relationship Some 2
Deafness-dystonia-optic neuronopathy syndrome (disorder) Interprets True Movement Inferred relationship Some 4
Frontotemporal dementia with parkinsonism-17 Interprets True Movement Inferred relationship Some 2
Dystonia 6 Interprets True Movement Inferred relationship Some 2
Spinal muscular atrophy with progressive myoclonic epilepsy (disorder) Interprets False Movement Inferred relationship Some 2
Lewy body dementia with behavioral disturbance Interprets True Movement Inferred relationship Some 5
Blepharospasm Interprets True Movement Inferred relationship Some 3
Proximal myopathy with extrapyramidal signs Interprets True Movement Inferred relationship Some 3
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Huntington disease-like 3 Interprets False Movement Inferred relationship Some 3
Infantile epileptic dyskinetic encephalopathy (disorder) Interprets True Movement Inferred relationship Some 3
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (disorder) Interprets True Movement Inferred relationship Some 3
Acquired torsion dystonia (disorder) Interprets True Movement Inferred relationship Some 3
Ataxia telangiectasia variant Interprets True Movement Inferred relationship Some 2
Benign paroxysmal tonic upgaze of childhood with ataxia (disorder) Interprets True Movement Inferred relationship Some 2
Progressive myoclonic epilepsy with dystonia Interprets True Movement Inferred relationship Some 3
Familial cortical myoclonus Interprets True Movement Inferred relationship Some 2
Morvan syndrome (disorder) Interprets True Movement Inferred relationship Some 3
Action myoclonus renal failure syndrome Interprets False Movement Inferred relationship Some 2
Hypermanganesemia with dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Hypermanganesemia with dystonia 2 (disorder) Interprets True Movement Inferred relationship Some 2
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) Interprets False Movement Inferred relationship Some 5
Hereditary essential tremor Interprets True Movement Inferred relationship Some 2
Dissociative neurological symptom disorder co-occurrent with dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Sleep-related movement disorder caused by drug Interprets True Movement Inferred relationship Some 3
Sleep-related movement disorder caused by substance Interprets False Movement Inferred relationship Some 3
Transient motor tic (disorder) Interprets True Movement Inferred relationship Some 3
Woodhouse Sakati syndrome Interprets True Movement Inferred relationship Some 5
Brain dopamine-serotonin vesicular transport disease (disorder) Interprets True Movement Inferred relationship Some 2
Primary dystonia type 4 (disorder) Interprets True Movement Inferred relationship Some 2
Primary dystonia type 13 (disorder) Interprets True Movement Inferred relationship Some 2
Autosomal dominant focal dystonia DYT25 type (disorder) Interprets True Movement Inferred relationship Some 2
Benign paroxysmal torticollis of infancy (disorder) Interprets True Movement Inferred relationship Some 4
Developmental malformation, deafness, dystonia syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Huntington disease-like 2 (disorder) Interprets False Movement Inferred relationship Some 4
Dystonia 16 (disorder) Interprets True Movement Inferred relationship Some 2
Ataxia due to mitochondrial mutations Interprets False Movement Inferred relationship Some 3
Secondary tic disorder (disorder) Interprets True Movement Inferred relationship Some 2
Tic due to developmental disorder (disorder) Interprets True Movement Inferred relationship Some 3
Segmental myoclonus (disorder) Interprets True Movement Inferred relationship Some 2
Primary tic disorder (disorder) Interprets True Movement Inferred relationship Some 2
Sialidosis type 1 (disorder) Interprets True Movement Inferred relationship Some 2
Sensorineural hearing loss, early graying, essential tremor syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Paroxysmal exertion-induced dyskinesia (disorder) Interprets True Movement Inferred relationship Some 3
McLeod neuroacanthocytosis syndrome (disorder) Interprets True Movement Inferred relationship Some 4
Infant epilepsy with migrant focal crisis (disorder) Interprets True Movement Inferred relationship Some 1
Hemidystonia hemiatrophy syndrome (disorder) Interprets True Movement Inferred relationship Some 3
Infection causing tic (disorder) Interprets True Movement Inferred relationship Some 1
Tic due to and following infection (disorder) Interprets True Movement Inferred relationship Some 4
Chorea co-occurrent and due to Huntington disease-like condition (disorder) Interprets False Movement Inferred relationship Some 3
Functional dystonia (disorder) Interprets True Movement Inferred relationship Some 3
Myoclonus, cerebellar ataxia, deafness syndrome Interprets True Movement Inferred relationship Some 1
Early-onset Lafora body disease (disorder) Interprets False Movement Inferred relationship Some 1
Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (disorder) Interprets True Movement Inferred relationship Some 4
Infantile convulsion and choreoathetosis syndrome (disorder) Interprets False Movement Inferred relationship Some 4

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