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255324009: Movement (observable entity)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. 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
    646347016 Movement (qualifier value) en Fully specified name Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
    1187242017 Movement, function (observable entity) en Fully specified name Inactive Only initial character 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

    0 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) false 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 False 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 False Movement Inferred relationship Some 2
    Primary dystonia type 2 (disorder) Interprets False Movement Inferred relationship Some 2
    Autosomal recessive dopa responsive dystonia (disorder) Interprets False Movement Inferred relationship Some 2
    Primary dystonia 21 (disorder) Interprets False Movement Inferred relationship Some 2
    Chronic hiccup (disorder) Interprets False Movement Inferred relationship Some 4
    Maternally inherited mitochondrial dystonia (disorder) Interprets False Movement Inferred relationship Some 2
    Benign adult familial myoclonic epilepsy (disorder) Interprets False Movement Inferred relationship Some 3
    Hereditary geniospasm (disorder) Interprets False Movement Inferred relationship Some 3
    Insomnia due to periodic limb movement disorder (disorder) Interprets False Movement Inferred relationship Some 3
    Dystonia of right hand (disorder) Interprets False Movement Inferred relationship Some 3
    Dystonia of left hand (disorder) Interprets False Movement Inferred relationship Some 3
    Shuddering attacks (disorder) Interprets False Movement Inferred relationship Some 2
    Sporadic olivopontocerebellar atrophy (disorder) Interprets False Movement Inferred relationship Some 2
    Focal dystonia (disorder) Interprets False Movement Inferred relationship Some 2
    Dystonia of head (disorder) Interprets False Movement Inferred relationship Some 2
    Spasmodic torticollis as late effect of trauma (disorder) Interprets False Movement Inferred relationship Some 4
    Spasmodic torticollis due to infection Interprets False Movement Inferred relationship Some 4
    Blepharospasm of right eyelid Interprets False Movement Inferred relationship Some 3
    Blepharospasm of left eyelid Interprets False Movement Inferred relationship Some 3
    Bilateral blepharospasm Interprets False Movement Inferred relationship Some 4
    Primary dystonia DYT17 type (disorder) Interprets False Movement Inferred relationship Some 2
    Dystonia aphonia syndrome (disorder) Interprets False 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 False 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 False Movement Inferred relationship Some 3
    Adult-onset cervical dystonia DYT23 type (disorder) Interprets False Movement Inferred relationship Some 2
    Familial infantile myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
    Familial congenital mirror movements Interprets False 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 False Movement Inferred relationship Some 2
    Movement disorder due to toxicity of substance Interprets False Movement Inferred relationship Some 3
    Idiopathic orofacial dystonia Interprets False Movement Inferred relationship Some 3
    Edentulous orofacial dystonia Interprets False Movement Inferred relationship Some 4
    Refractory myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
    Idiopathic familial dystonia Interprets False Movement Inferred relationship Some 2
    Idiopathic torsion dystonia (disorder) Interprets False Movement Inferred relationship Some 2
    Movement disorder Interprets False Movement Inferred relationship Some 1
    Apraxia as late effect of cerebrovascular disease Interprets False Movement Inferred relationship Some 3
    Apraxia due to cerebrovascular accident (disorder) Interprets False Movement Inferred relationship Some 2
    Psychosis co-occurrent and due to Parkinson's disease (disorder) Interprets False 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 False Movement Inferred relationship Some 2
    Cranial nerve palsy due to diabetes mellitus Interprets False Movement Inferred relationship Some 4
    Cranial nerve palsy due to type 1 diabetes mellitus Interprets False Movement Inferred relationship Some 4
    Cranial nerve palsy due to type 2 diabetes mellitus Interprets False Movement Inferred relationship Some 4
    Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder Interprets False Movement Inferred relationship Some 4
    Childhood-onset basal ganglia degeneration syndrome Interprets False Movement Inferred relationship Some 3
    Infantile-onset generalised dyskinesia with orofacial involvement Interprets False Movement Inferred relationship Some 2
    Facial diplegia with paresthesia (disorder) Interprets False Movement Inferred relationship Some 5
    Tic disorder due to rheumatic chorea Interprets False Movement Inferred relationship Some 3
    Tic disorder due to prion disease Interprets False Movement Inferred relationship Some 3
    Tic disorder due to encephalitis (disorder) Interprets False Movement Inferred relationship Some 3
    Tic disorder due to neurosyphilis (disorder) Interprets False Movement Inferred relationship Some 3
    Hyperphenylalanineaemia due to DNAJC12 deficiency Interprets False Movement Inferred relationship Some 2
    Tic disorder due to post-encephalitic syndrome Interprets False Movement Inferred relationship Some 3
    Parkinsonism following Mycoplasma infection (disorder) Interprets False Movement Inferred relationship Some 3
    Parkinsonism due to prion disease (disorder) Interprets False Movement Inferred relationship Some 3
    Nail dystrophy due to habit tic (disorder) Interprets False Movement Inferred relationship Some 5
    Callosity due to habit tic (disorder) Interprets False Movement Inferred relationship Some 5
    Callosity due to biting and/or chewing (disorder) Interprets False Movement Inferred relationship Some 4
    Akathisia caused by drug (disorder) Interprets False Movement Inferred relationship Some 2
    Akathisia Interprets False Movement Inferred relationship Some 2
    Acute akathisia caused by drug (disorder) Interprets False 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 False Movement Inferred relationship Some 2
    Parkinsonism caused by pesticide (disorder) Interprets False Movement Inferred relationship Some 2
    Dopa responsive dystonia due to sepiapterin reductase deficiency (disorder) Interprets False Movement Inferred relationship Some 3
    Dystonia due to Leigh syndrome Interprets False Movement Inferred relationship Some 2
    Bell's palsy Interprets False Movement Inferred relationship Some 1
    Paradoxical facial movements Interprets False Movement Inferred relationship Some 1
    Hyperexplexia Interprets False Movement Inferred relationship Some 3
    Oral dyskinesia Interprets False Movement Inferred relationship Some 2
    Excessive blinking - involuntary Interprets False Movement Inferred relationship Some 3
    Tremor of palate (finding) Interprets False Movement Inferred relationship Some 3
    Ataxia due to mitochondrial mutations Interprets False Movement Inferred relationship Some 2
    Tremor due to metabolic disorder Interprets False Movement Inferred relationship Some 2
    Tremor due to harmful pattern of substance use Interprets False Movement Inferred relationship Some 2
    Hereditary hyperekplexia (disorder) Interprets False Movement Inferred relationship Some 4
    Primary progressive freezing gait syndrome (disorder) Interprets False Movement Inferred relationship Some 1
    Primary orthostatic tremor (disorder) Interprets False Movement Inferred relationship Some 1
    Chronic hiccup (disorder) Interprets False Movement Inferred relationship Some 1
    Tardy left ulnar nerve palsy (finding) Interprets False Movement Inferred relationship Some 1
    Sporadic hyperekplexia (disorder) Interprets False Movement Inferred relationship Some 4
    Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) Interprets False Movement Inferred relationship Some 9
    Psychogenic movement disorder (disorder) Interprets False Movement Inferred relationship Some 1
    Severe oculo-renal-cerebellar syndrome (disorder) Interprets False Movement Inferred relationship Some 8
    Familial infantile bilateral striatal necrosis Interprets False Movement Inferred relationship Some 2
    Progressive myoclonic epilepsy type 7 Interprets False Movement Inferred relationship Some 3
    Autoimmune generalized polymyoclonus Interprets False Movement Inferred relationship Some 2
    Cerebellar ataxia with oculomotor apraxia type 4 (disorder) Interprets False Movement Inferred relationship Some 5
    Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) Interprets False Movement Inferred relationship Some 5
    Primary dystonia DYT27 type Interprets False Movement Inferred relationship Some 2
    Progressive myoclonic epilepsy type 9 Interprets False Movement Inferred relationship Some 3

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    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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