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255324009: Movement (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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

373 descendants. Search Descendants:

Expanded Value Set

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

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