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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
Morvan syndrome Interprets True Movement Inferred relationship Some 3
Action myoclonus renal failure syndrome Interprets False Movement Inferred relationship Some 2
Hypermanganesemia with dystonia Interprets True Movement Inferred relationship Some 2
Hypermanganesemia with dystonia 2 Interprets True Movement Inferred relationship Some 2
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome 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 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 True Movement Inferred relationship Some 3
Transient motor tic Interprets True Movement Inferred relationship Some 3
Woodhouse Sakati syndrome Interprets True Movement Inferred relationship Some 5
Brain dopamine-serotonin vesicular transport disease Interprets True Movement Inferred relationship Some 2
Primary dystonia DYT4 type Interprets True Movement Inferred relationship Some 2
Primary dystonia DYT13 type Interprets True Movement Inferred relationship Some 2
Autosomal dominant focal dystonia DYT25 type Interprets True Movement Inferred relationship Some 2
Benign paroxysmal torticollis of infancy Interprets True Movement Inferred relationship Some 4
Developmental malformation, deafness, dystonia syndrome Interprets True Movement Inferred relationship Some 5
Huntington disease-like 2 Interprets True Movement Inferred relationship Some 4
Dystonia 16 Interprets True Movement Inferred relationship Some 2
Ataxia due to mitochondrial mutations Interprets False Movement Inferred relationship Some 3
Secondary tic disorder Interprets True Movement Inferred relationship Some 2
Tic due to developmental disorder Interprets True Movement Inferred relationship Some 3
Segmental myoclonus Interprets True Movement Inferred relationship Some 2
Primary tic disorder Interprets True Movement Inferred relationship Some 2
Sialidosis type 1 Interprets True Movement Inferred relationship Some 2
Sensorineural hearing loss, early greying, essential tremor syndrome Interprets True Movement Inferred relationship Some 5
Paroxysmal exertion-induced dyskinesia Interprets True Movement Inferred relationship Some 3
McLeod neuroacanthocytosis syndrome Interprets True Movement Inferred relationship Some 4
Infant epilepsy with migrant focal crisis Interprets True Movement Inferred relationship Some 1
Hemidystonia hemiatrophy syndrome Interprets True Movement Inferred relationship Some 3
Infection causing tic Interprets True Movement Inferred relationship Some 1
Tic due to and following infection Interprets True Movement Inferred relationship Some 4
Chorea co-occurrent and due to Huntington disease-like condition Interprets True Movement Inferred relationship Some 3
Functional dystonia Interprets True Movement Inferred relationship Some 3
Myoclonus, cerebellar ataxia, deafness syndrome Interprets True Movement Inferred relationship Some 1
Early-onset Lafora body disease Interprets False Movement Inferred relationship Some 1
Olivopontocerebellar atrophy and deafness Interprets True Movement Inferred relationship Some 4
Infantile convulsion and choreoathetosis syndrome Interprets True Movement Inferred relationship Some 4
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity Interprets True Movement Inferred relationship Some 4
Primary progressive freezing gait Interprets False Movement Inferred relationship Some 2
Autosomal dominant dopa responsive dystonia Interprets True Movement Inferred relationship Some 2
Primary dystonia type 2 Interprets True Movement Inferred relationship Some 2
Autosomal recessive dopa responsive dystonia Interprets True Movement Inferred relationship Some 2
Primary dystonia 21 Interprets True Movement Inferred relationship Some 2
Chronic hiccups Interprets False Movement Inferred relationship Some 4
Maternally inherited mitochondrial dystonia Interprets True Movement Inferred relationship Some 2
Benign adult familial myoclonic epilepsy Interprets False Movement Inferred relationship Some 3
Hereditary geniospasm Interprets True Movement Inferred relationship Some 3
Insomnia co-occurrent and due to nocturnal myoclonus Interprets True Movement Inferred relationship Some 3
Dystonia of right hand Interprets True Movement Inferred relationship Some 3
Dystonia of left hand Interprets True Movement Inferred relationship Some 3
Shuddering attacks Interprets True Movement Inferred relationship Some 2
Sporadic olivopontocerebellar atrophy Interprets True Movement Inferred relationship Some 2
Focal dystonia Interprets True Movement Inferred relationship Some 2
Cranial dystonia Interprets True Movement Inferred relationship Some 2
Spasmodic torticolis as late effect of trauma Interprets True Movement Inferred relationship Some 4
Spasmodic torticollis due to infection Interprets True Movement Inferred relationship Some 4
Blepharospasm of right eyelid Interprets True Movement Inferred relationship Some 3
Blepharospasm of left eyelid Interprets True Movement Inferred relationship Some 3
Bilateral blepharospasm Interprets True Movement Inferred relationship Some 4
Primary dystonia DYT17 type Interprets True Movement Inferred relationship Some 2
Dystonia aphonia syndrome Interprets True Movement Inferred relationship Some 3
Huntington disease-like syndrome due to C9ORF72 expansions Interprets True Movement Inferred relationship Some 2
Tremor, nystagmus, duodenal ulcer syndrome Interprets True Movement Inferred relationship Some 5
Progressive myoclonic epilepsy type 5 Interprets False Movement Inferred relationship Some 3
Progressive myoclonic epilepsy type 6 Interprets False Movement Inferred relationship Some 3
Progressive myoclonic epilepsy type 3 Interprets False Movement Inferred relationship Some 3
Progressive myoclonic epilepsy type 8 Interprets False Movement Inferred relationship Some 3
Cranio-cervical dystonia with laryngeal and upper limb involvement Interprets True Movement Inferred relationship Some 3
Adult-onset cervical dystonia DYT23 type Interprets True Movement Inferred relationship Some 2
Familial infantile myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
Familial congenital mirror movements Interprets True Movement Inferred relationship Some 2
Huntington disease-like 1 Interprets True Movement Inferred relationship Some 2
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome Interprets True Movement Inferred relationship Some 2
Movement disorder due to toxicity of substance Interprets True Movement Inferred relationship Some 3
Idiopathic orofacial dystonia Interprets True Movement Inferred relationship Some 3
Edentulous orofacial dystonia Interprets True Movement Inferred relationship Some 4
Refractory myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
Idiopathic familial dystonia Interprets True Movement Inferred relationship Some 2
Primary torsion dystonia Interprets True Movement Inferred relationship Some 2
Movement disorder Interprets True Movement Inferred relationship Some 1
Apraxia as late effect of cerebrovascular disease Interprets True Movement Inferred relationship Some 3
Apraxia due to stroke Interprets True Movement Inferred relationship Some 2
Psychosis co-occurrent and due to Parkinson's disease Interprets True Movement Inferred relationship Some 2
Chorea due to and following encephalitis Interprets True Movement Inferred relationship Some 3
Ataxia due to disorder of immune function Interprets True Movement Inferred relationship Some 2
Cranial nerve palsy due to diabetes mellitus Interprets True Movement Inferred relationship Some 4
Cranial nerve palsy due to type 1 diabetes mellitus Interprets True Movement Inferred relationship Some 4
Cranial nerve palsy due to type 2 diabetes mellitus Interprets True Movement Inferred relationship Some 4
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder Interprets True Movement Inferred relationship Some 4
Childhood-onset basal ganglia degeneration syndrome Interprets True Movement Inferred relationship Some 3
Infantile-onset generalised dyskinesia with orofacial involvement Interprets True Movement Inferred relationship Some 2
Facial diplegia with paraesthesia Interprets True Movement Inferred relationship Some 5
Tic disorder due to rheumatic chorea Interprets True Movement Inferred relationship Some 3
Tic disorder due to prion disease Interprets True Movement Inferred relationship Some 3
Encephalitic tic disorder Interprets True Movement Inferred relationship Some 3
Neurosyphilitic tic disorder Interprets True Movement Inferred relationship Some 3
Hyperphenylalanineaemia due to DNAJC12 deficiency Interprets True Movement Inferred relationship Some 2
Tic disorder due to post-encephalitic syndrome Interprets True Movement Inferred relationship Some 3
Parkinsonism following Mycoplasma infection Interprets True Movement Inferred relationship Some 3
Parkinsonism due to prion disease Interprets True Movement Inferred relationship Some 3

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