FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

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
Hypotonic cerebral palsy Interprets True Movement Inferred relationship Some 4
Mirror movements Interprets True Movement Inferred relationship Some 2
Oral dystonia Interprets True Movement Inferred relationship Some 3
Oral dyskinesia Interprets False Movement Inferred relationship Some 3
Olivopontocerebellar atrophy with slow eye movement Interprets True Movement Inferred relationship Some 2
Olivopontocerebellar atrophy with blindness Interprets True Movement Inferred relationship Some 2
Kinesiogenic choreoathetosis Interprets True Movement Inferred relationship Some 2
Paroxysmal dystonia Interprets True Movement Inferred relationship Some 3
Sandifer syndrome Interprets True Movement Inferred relationship Some 5
Drug-induced acute dystonia Interprets True Movement Inferred relationship Some 3
Drug-induced tardive dystonia Interprets True Movement Inferred relationship Some 3
Idiopathic non-familial dystonia Interprets True Movement Inferred relationship Some 2
Isolated cervical dystonia Interprets True Movement Inferred relationship Some 2
Spasmodic retrocollis Interprets True Movement Inferred relationship Some 2
Isolated blepharospasm Interprets True Movement Inferred relationship Some 3
Meige syndrome Interprets True Movement Inferred relationship Some 2
Isolated oromandibular dystonia Interprets True Movement Inferred relationship Some 3
Posthemiplegic dystonia Interprets True Movement Inferred relationship Some 2
Occupational dystonia Interprets True Movement Inferred relationship Some 2
Diurnal dystonia Interprets True Movement Inferred relationship Some 2
Facial tic disorder Interprets True Movement Inferred relationship Some 3
Vocal tic disorder Interprets True Movement Inferred relationship Some 2
Motor tic disorder Interprets True Movement Inferred relationship Some 2
Gestural tic disorder Interprets True Movement Inferred relationship Some 3
Symptomatic myoclonus Interprets True Movement Inferred relationship Some 2
Postencephalitic myoclonus Interprets True Movement Inferred relationship Some 2
Drug-induced myoclonus Interprets True Movement Inferred relationship Some 3
Segmental cord myoclonus Interprets True Movement Inferred relationship Some 2
Palatal-tympanic myoclonus Interprets True Movement Inferred relationship Some 2
Hyoid myoclonus Interprets True Movement Inferred relationship Some 2
Opsoclonus-myoclonus syndrome Interprets True Movement Inferred relationship Some 2
Myoclonic astatic epilepsy Interprets False Movement Inferred relationship Some 2
Unverricht-Lundborg syndrome Interprets False Movement Inferred relationship Some 2
Lafora disease Interprets False Movement Inferred relationship Some 2
Myoclonic epilepsy with ragged red fibres Interprets True Movement Inferred relationship Some 4
Sleep-related dystonia Interprets True Movement Inferred relationship Some 2
Cluster tic syndrome Interprets True Movement Inferred relationship Some 2
Painful legs and moving toes Interprets True Movement Inferred relationship Some 4
Progressive myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
Senile dementia of the Lewy body type Interprets True Movement Inferred relationship Some 5
Autosomal dominant idiopathic familial dystonia Interprets True Movement Inferred relationship Some 2
Drug-induced tic Interprets True Movement Inferred relationship Some 3
Post-anoxic myoclonus Interprets True Movement Inferred relationship Some 3
Generalised dystonia Interprets True Movement Inferred relationship Some 2
Stapedial myoclonus Interprets True Movement Inferred relationship Some 3
Non-epileptic myoclonus Interprets True Movement Inferred relationship Some 2
Hemidystonia Interprets True Movement Inferred relationship Some 2
Reflex blepharospasm Interprets True Movement Inferred relationship Some 4
Severe myoclonic epilepsy in infancy Interprets False Movement Inferred relationship Some 2
Myoclonus associated with fever Interprets True Movement Inferred relationship Some 3
Myoclonic dystonia Interprets True Movement Inferred relationship Some 2
Habit tic Interprets True Movement Inferred relationship Some 3
Habit tic affecting skin Interprets True Movement Inferred relationship Some 3
Habit tic affecting hair Interprets True Movement Inferred relationship Some 3
Recurrent transient tic disorder Interprets True Movement Inferred relationship Some 4
Movement disorder due to medicine Interprets True Movement Inferred relationship Some 3
Drug-induced dystonia Interprets True Movement Inferred relationship Some 3
Drug-induced orofacial dyskinesia Interprets True Movement Inferred relationship Some 3
Benign neonatal sleep myoclonus Interprets True Movement Inferred relationship Some 3
Transient tic disorder Interprets True Movement Inferred relationship Some 3
Myoclonus of tensor tympani muscle Interprets True Movement Inferred relationship Some 3
Segmental dystonia Interprets True Movement Inferred relationship Some 2
Torsion dystonia Interprets True Movement Inferred relationship Some 2
Autoimmune opsoclonus myoclonus Interprets True Movement Inferred relationship Some 3
Acquired ataxia Interprets True Movement Inferred relationship Some 2
Ataxia due to chronic infection of central nervous system Interprets True Movement Inferred relationship Some 3
Dystonia caused by toxin Interprets True Movement Inferred relationship Some 2
Paroxysmal nonkinesigenic dyskinesia Interprets True Movement Inferred relationship Some 3
Paroxysmal kinesigenic dyskinesia Interprets True Movement Inferred relationship Some 3
Essential tremor Interprets True Movement Inferred relationship Some 2
Laryngeal dystonia Interprets True Movement Inferred relationship Some 3
Nocturnal myoclonus Interprets True Movement Inferred relationship Some 2
Organic sleep related movement disorder Interprets True Movement Inferred relationship Some 2
Brainstem myoclonus Interprets True Movement Inferred relationship Some 2
Refractory juvenile myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
Cerebral cortex myoclonus Interprets True Movement Inferred relationship Some 2
Spinal cord myoclonus Interprets True Movement Inferred relationship Some 2
Autosomal recessive idiopathic familial dystonia Interprets True Movement Inferred relationship Some 2
Ataxic cerebral palsy Interprets True Movement Inferred relationship Some 4
Congenital athetosis Interprets True Movement Inferred relationship Some 2
Non-spastic cerebral palsy Interprets True Movement Inferred relationship Some 4
Progressive myoclonus epilepsy with ataxia Interprets False Movement Inferred relationship Some 2
Huntington disease-like syndrome Interprets True Movement Inferred relationship Some 2
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis Interprets True Movement Inferred relationship Some 2
Deafness-dystonia-optic neuronopathy syndrome Interprets True Movement Inferred relationship Some 4
Frontotemporal dementia with parkinsonism-17 Interprets True Movement Inferred relationship Some 2
THAP1 dystonia Interprets True Movement Inferred relationship Some 2
Spinal muscular atrophy with progressive myoclonic epilepsy Interprets False Movement Inferred relationship Some 2
Lewy body dementia with behavioural disturbance Interprets True Movement Inferred relationship Some 5
Blepharospasm Interprets True Movement Inferred relationship Some 3
Proximal myopathy with extrapyramidal signs Interprets True Movement Inferred relationship Some 3
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome Interprets True Movement Inferred relationship Some 5
Huntington disease-like 3 Interprets True Movement Inferred relationship Some 3
Infantile epileptic dyskinetic encephalopathy Interprets True Movement Inferred relationship Some 3
Steroid-responsive encephalopathy associated with autoimmune thyroiditis Interprets True Movement Inferred relationship Some 3
Acquired torsion dystonia Interprets True Movement Inferred relationship Some 3
Ataxia telangiectasia variant Interprets True Movement Inferred relationship Some 2
Benign paroxysmal tonic upgaze of childhood with ataxia Interprets True Movement Inferred relationship Some 2
Progressive myoclonic epilepsy with dystonia Interprets True Movement Inferred relationship Some 3
Familial myoclonus of cerebral cortex Interprets True Movement Inferred relationship Some 2
Morvan syndrome Interprets True Movement Inferred relationship Some 3

Start Previous Page 6 of 15 Next End

Reference Sets

Observable entity foundation reference set

Back to Start