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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
380509014 Movement en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1187242017 Movement, function (observable entity) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2528848014 Movement (observable entity) en Fully specified name Active 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
42051000077112 mouvement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
42051000077112 mouvement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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 Existential restriction modifier (core metadata concept)
Movement Is a Process (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Painful legs and moving toes Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Progressive myoclonic epilepsy (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Senile dementia of the Lewy body type Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 5
Autosomal dominant idiopathic familial dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Tic caused by drug Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Post-anoxic myoclonus Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Generalized dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Myoclonus of stapedius muscle (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Non-epileptic myoclonus (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Hemidystonia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Reflex blepharospasm (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Severe myoclonic epilepsy in infancy Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Myoclonus associated with fever Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Myoclonic dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Habit tic (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Habit tic affecting skin (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Habit tic affecting hair (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Recurrent transient tic disorder Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Medication-induced movement disorder (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Drug-induced dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Drug-induced orofacial dyskinesia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Benign neonatal sleep myoclonus (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Transient tic disorder Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Myoclonus of tensor tympani muscle Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Segmental dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Torsion dystonia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Autoimmune opsoclonus myoclonus (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Acquired ataxia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Ataxia due to chronic infection of central nervous system (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Toxic dystonia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Paroxysmal nonkinesigenic dyskinesia (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Paroxysmal kinesigenic dyskinesia Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Essential tremor (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Laryngeal dystonia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
myoclonie nocturne Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Organic sleep related movement disorder (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Brainstem myoclonus Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Refractory juvenile myoclonic epilepsy Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Cerebral cortex myoclonus (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Spinal cord myoclonus Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive idiopathic familial dystonia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital athetosis (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
A less common type of cerebral palsy defined by decreased and/or fluctuating muscle tone; multiple forms of non-spastic cerebral palsy are each characterised by particular impairments; one of the main characteristics of non-spastic cerebral palsy is involuntary movement. Subtypes include ataxic and dyskinetic forms. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Progressive myoclonus epilepsy with ataxia (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Huntington disease-like syndrome Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypermanganesemia with dystonia, polycythemia, and cirrhosis Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Deafness-dystonia-optic neuronopathy syndrome (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Frontotemporal dementia with parkinsonism-17 Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Dystonia 6 Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Spinal muscular atrophy with progressive myoclonic epilepsy Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Lewy body dementia with behavioral disturbance (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 5
Blepharospasm Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Proximal myopathy with extrapyramidal signs Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare, genetic, neurological disorder characterized by intrauterine growth retardation, failure to thrive, infantile onset of sensorineural deafness, severe global developmental delay or absent psychomotor development, paraplegia or quadriplegia with dystonia and pyramidal signs, microcephaly, ocular abnormalities (strabismus, optic atrophy), mildly dysmorphic features (deep-set eyes, prominent nasal bridge, micrognathia), seizures and abnormalities of brain morphology (hypomyelinating white matter changes, cerebral atrophy). Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 5
Huntington disease-like 3 Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Infantile epileptic dyskinetic encephalopathy Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Acquired torsion dystonia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Ataxia telangiectasia variant Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Benign paroxysmal tonic upgaze of childhood with ataxia is a rare paroxysmal movement disorder characterized by episodes of sustained, conjugate, upward deviation of the eyes and down beating saccades in attempted downgaze (with preserved horizontal eye movements) which is accompanied by ataxic symptomatology (unsteady gait, lack of balance and movement coordination disturbances) in an otherwise healthy individual. Bilateral vertical nystagmus is associated. Symptoms generally disappear spontaneously within 1-2 years after onset. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Progressive myoclonic epilepsy with dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial myoclonus of cerebral cortex (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Morvan syndrome (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Action myoclonus renal failure syndrome Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypermanganesemia with dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypermanganesemia with dystonia 2 (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary essential tremor Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Dissociative neurological symptom disorder co-occurrent with dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Sleep-related movement disorder caused by drug Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Sleep-related movement disorder caused by substance Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Transient motor tic (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Woodhouse Sakati syndrome Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 5
Brain dopamine-serotonin vesicular transport disease (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Primary dystonia type 4 (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Primary dystonia type 13 Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of focal dystonia characterized by cervical, laryngeal and hand-forearm dystonia. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare, transient paroxysmal dystonia characterized by onset of recurrent episodes of torticollis posturing of the head between infancy and early-childhood. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Developmental malformations-deafness-dystonia syndrome is characterized by the association of midline malformations, sensory hearing loss, and a delayed-onset generalized dystonia syndrome. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 5
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia). Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Ataxia due to mitochondrial mutations Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Secondary tic disorder (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Tic due to developmental disorder Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Segmental myoclonus (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Primary tic disorder Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Sialidosis type 1 (ST-1) is a very rare lysosomal storage disease, and is the normosomatic form of sialidosis, characterized by gait abnormalities, progressive visual loss, bilateral macular cherry red spots and myoclonic epilepsy and ataxia, that usually presents in the second to third decade of life. Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 2
Sensorineural hearing loss, early greying, essential tremor syndrome Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 5
Paroxysmal exertion-induced dyskinesia Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
McLeod neuroacanthocytosis syndrome (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Infant epilepsy with migrant focal crisis (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 1
Hemidystonia hemiatrophy syndrome (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Infection causing tic (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 1
Tic due to and following infection Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Chorea co-occurrent and due to Huntington disease-like condition (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Functional dystonia (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 3
Myoclonus, cerebellar ataxia, deafness syndrome Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 1
Early-onset Lafora body disease (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 1
Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (disorder) Interprets True Movement Inferred relationship Existential restriction modifier (core metadata concept) 4
Infantile convulsion and choreoathetosis syndrome (disorder) Interprets False Movement Inferred relationship Existential restriction modifier (core metadata concept) 4

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