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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
Infantile convulsion and choreoathetosis syndrome (disorder) Interprets False Movement Inferred relationship Some 4
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder) Interprets True Movement Inferred relationship Some 4
Primary progressive freezing gait syndrome (disorder) Interprets False Movement Inferred relationship Some 2
Autosomal dominant dopa responsive dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Primary dystonia type 2 (disorder) Interprets True Movement Inferred relationship Some 2
Autosomal recessive dopa responsive dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Primary dystonia 21 (disorder) Interprets True Movement Inferred relationship Some 2
Chronic hiccup (disorder) Interprets False Movement Inferred relationship Some 4
Maternally inherited mitochondrial dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Benign adult familial myoclonic epilepsy (disorder) Interprets False Movement Inferred relationship Some 3
Hereditary geniospasm (disorder) Interprets True Movement Inferred relationship Some 3
Insomnia due to periodic limb movement disorder (disorder) Interprets True Movement Inferred relationship Some 3
Dystonia of right hand (disorder) Interprets True Movement Inferred relationship Some 3
Dystonia of left hand (disorder) Interprets True Movement Inferred relationship Some 3
Shuddering attacks (disorder) Interprets True Movement Inferred relationship Some 2
Sporadic olivopontocerebellar atrophy (disorder) Interprets True Movement Inferred relationship Some 2
Focal dystonia (disorder) Interprets True Movement Inferred relationship Some 2
Dystonia of head (disorder) Interprets True Movement Inferred relationship Some 2
Spasmodic torticollis as late effect of trauma (disorder) 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 (disorder) Interprets True Movement Inferred relationship Some 2
Dystonia aphonia syndrome (disorder) Interprets True Movement Inferred relationship Some 3
Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) Interprets False Movement Inferred relationship Some 2
Tremor, nystagmus, duodenal ulcer syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Progressive myoclonic epilepsy type 5 (disorder) Interprets False Movement Inferred relationship Some 3
Progressive myoclonic epilepsy type 6 (disorder) Interprets False Movement Inferred relationship Some 3
Progressive myoclonic epilepsy type 3 Interprets False Movement Inferred relationship Some 3
Progressive myoclonic epilepsy type 8 (disorder) 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 (disorder) 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 (disorder) Interprets False Movement Inferred relationship Some 2
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder) 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
Idiopathic torsion dystonia (disorder) 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 cerebrovascular accident (disorder) Interprets True Movement Inferred relationship Some 2
Psychosis co-occurrent and due to Parkinson's disease (disorder) Interprets True Movement Inferred relationship Some 2
Chorea due to and following encephalitis Interprets False Movement Inferred relationship Some 3
Ataxia due to disorder of immune function (disorder) 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 paresthesia (disorder) 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
Tic disorder due to encephalitis (disorder) Interprets True Movement Inferred relationship Some 3
Tic disorder due to neurosyphilis (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 (disorder) Interprets True Movement Inferred relationship Some 3
Parkinsonism due to prion disease (disorder) Interprets True Movement Inferred relationship Some 3
Nail dystrophy due to habit tic (disorder) Interprets True Movement Inferred relationship Some 5
Callosity due to habit tic (disorder) Interprets True Movement Inferred relationship Some 5
Callosity due to biting and/or chewing (disorder) Interprets True Movement Inferred relationship Some 4
Akathisia caused by drug (disorder) Interprets True Movement Inferred relationship Some 2
Akathisia Interprets True Movement Inferred relationship Some 2
Acute akathisia caused by drug (disorder) Interprets True Movement Inferred relationship Some 4
Classical pantothenate kinase associated neurodegeneration Interprets False Movement Inferred relationship Some 2
Atypical pantothenate kinase associated neurodegeneration (disorder) Interprets False Movement Inferred relationship Some 2
Toxin-induced parkinsonism Interprets True Movement Inferred relationship Some 2
Parkinsonism caused by pesticide (disorder) Interprets True Movement Inferred relationship Some 2
Dopa responsive dystonia due to sepiapterin reductase deficiency (disorder) Interprets True Movement Inferred relationship Some 3
Dystonia due to Leigh syndrome Interprets True Movement Inferred relationship Some 2
Bell's palsy Interprets False Movement Inferred relationship Some 1
Paradoxical facial movements Interprets True Movement Inferred relationship Some 1
Hyperexplexia Interprets True Movement Inferred relationship Some 3
Oral dyskinesia Interprets True Movement Inferred relationship Some 2
Excessive blinking - involuntary Interprets True Movement Inferred relationship Some 3
Tremor of palate (finding) Interprets True Movement Inferred relationship Some 3
Ataxia due to mitochondrial mutations Interprets True Movement Inferred relationship Some 2
Tremor due to metabolic disorder Interprets True Movement Inferred relationship Some 2
Tremor due to substance abuse Interprets True Movement Inferred relationship Some 2
Hereditary hyperekplexia (disorder) Interprets True Movement Inferred relationship Some 4
Primary progressive freezing gait syndrome (disorder) Interprets True Movement Inferred relationship Some 1
Primary orthostatic tremor (disorder) Interprets True Movement Inferred relationship Some 1
Chronic hiccup (disorder) Interprets True Movement Inferred relationship Some 1
Tardy left ulnar nerve palsy (finding) Interprets True Movement Inferred relationship Some 1
Sporadic hyperekplexia (disorder) Interprets True Movement Inferred relationship Some 4
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) Interprets True Movement Inferred relationship Some 9
Psychogenic movement disorder (disorder) Interprets True Movement Inferred relationship Some 1
Severe oculo-renal-cerebellar syndrome (disorder) Interprets False Movement Inferred relationship Some 8
Familial infantile bilateral striatal necrosis Interprets True Movement Inferred relationship Some 2
Progressive myoclonic epilepsy type 7 Interprets True Movement Inferred relationship Some 3
Autoimmune generalized polymyoclonus Interprets True Movement Inferred relationship Some 2
Cerebellar ataxia with oculomotor apraxia type 4 (disorder) Interprets True Movement Inferred relationship Some 5
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Primary dystonia DYT27 type Interprets True Movement Inferred relationship Some 2
Progressive myoclonic epilepsy type 9 Interprets True Movement Inferred relationship Some 3

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