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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
Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss Interprets True Movement Inferred relationship Existential restriction modifier 4
Infantile convulsion and choreoathetosis syndrome Interprets True Movement Inferred relationship Existential restriction modifier 4
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity Interprets True Movement Inferred relationship Existential restriction modifier 4
Primary progressive freezing gait syndrome Interprets False Movement Inferred relationship Existential restriction modifier 2
Autosomal dominant dopa responsive dystonia Interprets True Movement Inferred relationship Existential restriction modifier 2
Primary dystonia type 2 Interprets True Movement Inferred relationship Existential restriction modifier 2
Autosomal recessive dopa responsive dystonia Interprets True Movement Inferred relationship Existential restriction modifier 2
Primary dystonia 21 Interprets True Movement Inferred relationship Existential restriction modifier 2
Chronic hiccup Interprets False Movement Inferred relationship Existential restriction modifier 4
Maternally inherited mitochondrial dystonia Interprets True Movement Inferred relationship Existential restriction modifier 2
Benign adult familial myoclonic epilepsy Interprets False Movement Inferred relationship Existential restriction modifier 3
Hereditary geniospasm Interprets True Movement Inferred relationship Existential restriction modifier 3
Insomnia co-occurrent and due to nocturnal myoclonus Interprets True Movement Inferred relationship Existential restriction modifier 3
Dystonia of right hand Interprets True Movement Inferred relationship Existential restriction modifier 3
Dystonia of left hand Interprets True Movement Inferred relationship Existential restriction modifier 3
Shuddering attacks Interprets True Movement Inferred relationship Existential restriction modifier 2
Sporadic olivopontocerebellar atrophy Interprets True Movement Inferred relationship Existential restriction modifier 2
Focal dystonia Interprets True Movement Inferred relationship Existential restriction modifier 2
Dystonia of head Interprets True Movement Inferred relationship Existential restriction modifier 2
Spasmodic torticollis as late effect of trauma Interprets True Movement Inferred relationship Existential restriction modifier 4
Spasmodic torticollis due to infection Interprets True Movement Inferred relationship Existential restriction modifier 4
Blepharospasm of right eyelid Interprets True Movement Inferred relationship Existential restriction modifier 3
Blepharospasm of left eyelid Interprets True Movement Inferred relationship Existential restriction modifier 3
Blepharospasm of bilateral eyelids Interprets True Movement Inferred relationship Existential restriction modifier 4
Primary dystonia DYT17 type Interprets True Movement Inferred relationship Existential restriction modifier 2
Dystonia aphonia syndrome Interprets True Movement Inferred relationship Existential restriction modifier 3
Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions Interprets True Movement Inferred relationship Existential restriction modifier 2
Tremor, nystagmus, duodenal ulcer syndrome Interprets True Movement Inferred relationship Existential restriction modifier 5
Progressive myoclonic epilepsy type 5 Interprets False Movement Inferred relationship Existential restriction modifier 3
Progressive myoclonic epilepsy type 6 Interprets False Movement Inferred relationship Existential restriction modifier 3
Progressive myoclonic epilepsy type 3 Interprets False Movement Inferred relationship Existential restriction modifier 3
Progressive myoclonic epilepsy type 8 Interprets False Movement Inferred relationship Existential restriction modifier 3
Cranio-cervical dystonia with laryngeal and upper limb involvement Interprets True Movement Inferred relationship Existential restriction modifier 3
Adult-onset cervical dystonia DYT23 type Interprets True Movement Inferred relationship Existential restriction modifier 2
Familial infantile myoclonic epilepsy Interprets False Movement Inferred relationship Existential restriction modifier 2
Familial congenital mirror movements Interprets True Movement Inferred relationship Existential restriction modifier 2
Huntington disease-like 1 Interprets True Movement Inferred relationship Existential restriction modifier 2
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome Interprets True Movement Inferred relationship Existential restriction modifier 2
Movement disorder due to toxicity of substance Interprets True Movement Inferred relationship Existential restriction modifier 3
Idiopathic orofacial dystonia Interprets True Movement Inferred relationship Existential restriction modifier 3
Edentulous orofacial dystonia Interprets True Movement Inferred relationship Existential restriction modifier 4
Refractory myoclonic epilepsy Interprets False Movement Inferred relationship Existential restriction modifier 2
Idiopathic familial dystonia Interprets True Movement Inferred relationship Existential restriction modifier 2
Idiopathic torsion dystonia Interprets True Movement Inferred relationship Existential restriction modifier 2
Movement disorder Interprets True Movement Inferred relationship Existential restriction modifier 1
Apraxia as late effect of cerebrovascular disease Interprets True Movement Inferred relationship Existential restriction modifier 3
Apraxia due to cerebrovascular accident Interprets True Movement Inferred relationship Existential restriction modifier 2
Psychosis co-occurrent and due to Parkinson's disease Interprets True Movement Inferred relationship Existential restriction modifier 2
Chorea due to and following encephalitis Interprets True Movement Inferred relationship Existential restriction modifier 3
Ataxia due to disorder of immune function Interprets True Movement Inferred relationship Existential restriction modifier 2
Cranial nerve palsy due to diabetes mellitus Interprets True Movement Inferred relationship Existential restriction modifier 4
Cranial nerve palsy due to type 1 diabetes mellitus Interprets True Movement Inferred relationship Existential restriction modifier 4
Cranial nerve palsy due to type 2 diabetes mellitus Interprets True Movement Inferred relationship Existential restriction modifier 4
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder Interprets True Movement Inferred relationship Existential restriction modifier 4
Childhood-onset basal ganglia degeneration syndrome Interprets True Movement Inferred relationship Existential restriction modifier 3
Infantile-onset generalized dyskinesia with orofacial involvement Interprets True Movement Inferred relationship Existential restriction modifier 2
Facial diplegia with paresthesia Interprets True Movement Inferred relationship Existential restriction modifier 5
Tic disorder due to rheumatic chorea Interprets True Movement Inferred relationship Existential restriction modifier 3
Tic disorder due to prion disease Interprets True Movement Inferred relationship Existential restriction modifier 3
Tic disorder due to encephalitis Interprets True Movement Inferred relationship Existential restriction modifier 3
Tic disorder due to neurosyphilis Interprets True Movement Inferred relationship Existential restriction modifier 3
Hyperphenylalaninemia due to DnaJ heat shock protein family (Hsp40) member C12 deficiency Interprets True Movement Inferred relationship Existential restriction modifier 2
Tic disorder due to post-encephalitic syndrome Interprets True Movement Inferred relationship Existential restriction modifier 3
Parkinsonism following Mycoplasma infection Interprets True Movement Inferred relationship Existential restriction modifier 3
Parkinsonism due to prion disease Interprets True Movement Inferred relationship Existential restriction modifier 3
Nail dystrophy due to habit tic Interprets True Movement Inferred relationship Existential restriction modifier 5
Callosity due to habit tic Interprets True Movement Inferred relationship Existential restriction modifier 5
Callosity caused by biting and/or chewing Interprets True Movement Inferred relationship Existential restriction modifier 4
Akathisia caused by drug Interprets True Movement Inferred relationship Existential restriction modifier 2
Akathisia Interprets True Movement Inferred relationship Existential restriction modifier 2
Acute akathisia caused by drug Interprets True Movement Inferred relationship Existential restriction modifier 4
Classical pantothenate kinase associated neurodegeneration Interprets True Movement Inferred relationship Existential restriction modifier 2
Atypical pantothenate kinase associated neurodegeneration Interprets True Movement Inferred relationship Existential restriction modifier 2
Parkinsonism caused by toxin Interprets True Movement Inferred relationship Existential restriction modifier 2
Parkinsonism caused by pesticide Interprets True Movement Inferred relationship Existential restriction modifier 2
Dopa responsive dystonia due to sepiapterin reductase deficiency Interprets True Movement Inferred relationship Existential restriction modifier 3
Dystonia due to Leigh syndrome Interprets True Movement Inferred relationship Existential restriction modifier 2
Bell's palsy Interprets False Movement Inferred relationship Existential restriction modifier 1
Paradoxical facial movements Interprets True Movement Inferred relationship Existential restriction modifier 1
Hyperexplexia Interprets True Movement Inferred relationship Existential restriction modifier 3
Oral dyskinesia Interprets True Movement Inferred relationship Existential restriction modifier 2
Excessive blinking - involuntary Interprets True Movement Inferred relationship Existential restriction modifier 3
Tremor of palate Interprets True Movement Inferred relationship Existential restriction modifier 3
Ataxia due to mitochondrial mutations Interprets True Movement Inferred relationship Existential restriction modifier 2
Tremor due to metabolic disorder Interprets True Movement Inferred relationship Existential restriction modifier 2
Tremor due to substance abuse Interprets True Movement Inferred relationship Existential restriction modifier 2
Hereditary hyperekplexia Interprets True Movement Inferred relationship Existential restriction modifier 4
Primary progressive freezing gait syndrome Interprets True Movement Inferred relationship Existential restriction modifier 1
Primary orthostatic tremor Interprets True Movement Inferred relationship Existential restriction modifier 1
Chronic hiccup Interprets True Movement Inferred relationship Existential restriction modifier 1
Tardy left ulnar nerve palsy Interprets True Movement Inferred relationship Existential restriction modifier 1
Sporadic hyperekplexia Interprets True Movement Inferred relationship Existential restriction modifier 4
Congenital ichthyosis, microcephalus, tetraplegia syndrome Interprets True Movement Inferred relationship Existential restriction modifier 9
Psychogenic movement disorder Interprets True Movement Inferred relationship Existential restriction modifier 1
Severe oculo-renal-cerebellar syndrome Interprets True Movement Inferred relationship Existential restriction modifier 8
Familial infantile bilateral striatal necrosis Interprets True Movement Inferred relationship Existential restriction modifier 2
Progressive myoclonic epilepsy type 7 Interprets True Movement Inferred relationship Existential restriction modifier 3
Autoimmune generalized polymyoclonus Interprets True Movement Inferred relationship Existential restriction modifier 2
Cerebellar ataxia with oculomotor apraxia type 4 Interprets True Movement Inferred relationship Existential restriction modifier 5
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Interprets True Movement Inferred relationship Existential restriction modifier 5
Primary dystonia type 27 Interprets True Movement Inferred relationship Existential restriction modifier 2

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