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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
    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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    mouvement Is a Gross motor functions (observable entity) false Inferred relationship Some
    mouvement Is a Process (observable entity) false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Juvenile neuronal ceroid lipofuscinosis Interprets False mouvement Inferred relationship Some 2
    Spastic pseudobulbar dysphonia Interprets False mouvement Inferred relationship Some 3
    Mixed flaccid-spastic pseudobulbar dysphonia Interprets False mouvement Inferred relationship Some 3
    Chorea due to immunoglobulin A vasculitis (disorder) Interprets False mouvement Inferred relationship Some 2
    Pallidonigrospinal degeneration Interprets False mouvement Inferred relationship Some 2
    Tic of organic origin Interprets False mouvement Inferred relationship Some 2
    dystonie de torsion symptomatique Interprets False mouvement Inferred relationship Some 2
    Adductor spastic dysphonia of organic voice tremor Interprets False mouvement Inferred relationship Some 3
    Pallidonigral degeneration Interprets False mouvement Inferred relationship Some 2
    Adductor spastic dysphonia of dystonia Interprets False mouvement Inferred relationship Some 3
    Dysmorphic sialidosis with renal involvement Interprets False mouvement Inferred relationship Some 4
    Dubini's chorea Interprets False mouvement Inferred relationship Some 2
    Neuroleptic-induced acute dystonia Interprets False mouvement Inferred relationship Some 4
    Adductor spastic dysphonia of musculoskeletal tension reaction Interprets False mouvement Inferred relationship Some 3
    Dysmorphic sialidosis, infantile form Interprets False mouvement Inferred relationship Some 4
    Organic writer's cramp Interprets False mouvement Inferred relationship Some 2
    Dysmorphic sialidosis Interprets False mouvement Inferred relationship Some 3
    Dystonia lenticularis Interprets False mouvement Inferred relationship Some 2
    Posthemiplegic athetosis Interprets False mouvement Inferred relationship Some 2
    Acute akathisia caused by neuroleptic (disorder) Interprets False mouvement Inferred relationship Some 4
    Dysphonia of Gilles de la Tourette's syndrome Interprets False mouvement Inferred relationship Some 3
    Myoclonic seizure Interprets False mouvement Inferred relationship Some 2
    Sialidosis is a lysosomal storage disease, belonging to the group of oligosaccharidoses or glycoproteinoses, with a wide clinical spectrum that is divided into two main clinical subtypes: sialidosis type I, the milder, non-dysmorphic form of the disease characterized by gait abnormalities, progressive visual loss, bilateral macular cherry red spots and myoclonus, that presents in adolescence or adulthood (second or third decade of life); and sialidosis type II the more severe, early onset form, characterized by a progressive and severe mucopolysaccharidosis-like phenotype with coarse facies, visceromegaly, dysostosis multiplex, and developmental delay. Bilateral macular cherry red spots are also present. Sialidosis type II has been further divided into congenital (with hydrops fetalis), infantile and juvenile presentations. Interprets False mouvement Inferred relationship Some 3
    Grimaces Interprets False mouvement Inferred relationship Some 2
    Dysphonia of palatopharyngolaryngeal myoclonus Interprets False mouvement Inferred relationship Some 6
    Abductor spastic dysphonia Interprets False mouvement Inferred relationship Some 3
    Medication-induced postural tremor Interprets False mouvement Inferred relationship Some 3
    Progressive cerebellar tremor Interprets False mouvement Inferred relationship Some 2
    Pallidopontonigral degeneration Interprets False mouvement Inferred relationship Some 2
    Diffuse Lewy body disease with spongiform cortical change Interprets False mouvement Inferred relationship Some 4
    Choreoathetosis Interprets False mouvement Inferred relationship Some 2
    Juvenile paralysis agitans of Hunt Interprets False mouvement Inferred relationship Some 2
    Early myoclonic encephalopathy Interprets False mouvement Inferred relationship Some 2
    Athetosis Interprets False mouvement Inferred relationship Some 2
    Psychogenic adductor spastic dysphonia Interprets False mouvement Inferred relationship Some 4
    Dysmorphic sialidosis, congenital form Interprets False mouvement Inferred relationship Some 2
    Spastic dysphonia Interprets False mouvement Inferred relationship Some 3
    Idiopathic adductor spastic dysphonia Interprets False mouvement Inferred relationship Some 3
    Birnbaum's syndrome Interprets False mouvement Inferred relationship Some 2
    Neurologic adductor spastic dysphonia Interprets False mouvement Inferred relationship Some 3
    Orofacial dyskinesia Interprets False mouvement Inferred relationship Some 2
    Paroxysmal choreoathetosis Interprets False mouvement Inferred relationship Some 3
    Neuroleptic malignant syndrome Interprets False mouvement Inferred relationship Some 3
    Dystonia Interprets False mouvement Inferred relationship Some 2
    Corticobasal degeneration Interprets False mouvement Inferred relationship Some 3
    Pallidoluysian degeneration Interprets False mouvement Inferred relationship Some 2
    Athetosis with rigidity (disorder) Interprets False mouvement Inferred relationship Some 2
    Adductor spastic dysphonia Interprets False mouvement Inferred relationship Some 3
    Gilles de la Tourette's syndrome Interprets False mouvement Inferred relationship Some 2
    A rare neurological disorder comprising fluctuating trunk and limb stiffness, painful muscle spasms, task-specific phobia related to walking, an exaggerated startle response, and often ankylosing deformities such as fixed lumbar hyperlordosis. Interprets False mouvement Inferred relationship Some 3
    Athetosis with spastic paraplegia Interprets False mouvement Inferred relationship Some 4
    A type of epilepsy that presents with myoclonic epileptic seizures, usually between 10 and 24 years of age, in an otherwise normal adolescent or adult. Generalized tonic-clonic seizures occur in greater than 90 percent of individuals and absence seizures occur in a third. Seizures typically occur shortly after waking and when tired. Sleep deprivation is an important provoking factor. Photosensitivity is common. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalized spike-wave and polyspike-wave and a normal background. Interprets False mouvement Inferred relationship Some 2
    Chronic motor tic disorder Interprets False mouvement Inferred relationship Some 3
    Transient tic disorder, single episode Interprets False mouvement Inferred relationship Some 3
    Palatal myoclonus Interprets False mouvement Inferred relationship Some 4
    Tic disorder Interprets False mouvement Inferred relationship Some 2
    Pigmentary pallidal degeneration Interprets False mouvement Inferred relationship Some 2
    Chronic progressive non-hereditary chorea Interprets False mouvement Inferred relationship Some 3
    Dysmorphic sialidosis, juvenile form Interprets False mouvement Inferred relationship Some 4
    Myoclonic disorder Interprets False mouvement Inferred relationship Some 2
    Progressive pyramidopallidal degeneration Interprets False mouvement Inferred relationship Some 2
    Transient childhood tic (disorder) Interprets False mouvement Inferred relationship Some 4
    Fragments of torsion dystonia Interprets False mouvement Inferred relationship Some 2
    A form of non-spastic cerebral palsy with decreased muscle tone, noticeably floppy muscles with poor or no head control. Interprets False mouvement Inferred relationship Some 4
    Mirror movements Interprets False mouvement Inferred relationship Some 2
    Oral dystonia Interprets False mouvement Inferred relationship Some 3
    Oral dyskinesia Interprets False mouvement Inferred relationship Some 3
    Olivopontocerebellar atrophy with slow eye movement Interprets False mouvement Inferred relationship Some 2
    Olivopontocerebellar atrophy with blindness Interprets False mouvement Inferred relationship Some 2
    Kinesiogenic choreoathetosis Interprets False mouvement Inferred relationship Some 2
    Paroxysmal dystonia Interprets False mouvement Inferred relationship Some 3
    A paroxysmal dystonic movement disorder occurring in association with gastro-oesophageal reflux, and, in some cases, hiatal hernia. The prevalence is unknown. Onset usually occurs during infancy or early childhood. The dystonic movements are characterised by abnormal posturing of the head and neck (torticollis) and severe arching of the spine. The dystonic movements are clearly associated with gastro-oesophageal reflux but the pathophysiological mechanism is not clearly understood. Interprets False mouvement Inferred relationship Some 5
    Drug-induced acute dystonia Interprets False mouvement Inferred relationship Some 3
    Drug-induced tardive dystonia Interprets False mouvement Inferred relationship Some 3
    Idiopathic non-familial dystonia Interprets False mouvement Inferred relationship Some 2
    Isolated cervical dystonia Interprets False mouvement Inferred relationship Some 2
    Spasmodic retrocollis Interprets False mouvement Inferred relationship Some 2
    Isolated blepharospasm Interprets False mouvement Inferred relationship Some 3
    Meige syndrome Interprets False mouvement Inferred relationship Some 2
    Isolated oromandibular dystonia Interprets False mouvement Inferred relationship Some 3
    Posthemiplegic dystonia Interprets False mouvement Inferred relationship Some 2
    Occupational dystonia Interprets False mouvement Inferred relationship Some 2
    Diurnal dystonia Interprets False mouvement Inferred relationship Some 2
    Facial tic disorder Interprets False mouvement Inferred relationship Some 3
    Vocal tic disorder Interprets False mouvement Inferred relationship Some 2
    Motor tic disorder Interprets False mouvement Inferred relationship Some 2
    Gestural tic disorder Interprets False mouvement Inferred relationship Some 3
    myoclonies symptomatiques Interprets False mouvement Inferred relationship Some 2
    Postencephalitic myoclonus Interprets False mouvement Inferred relationship Some 2
    Drug-induced myoclonus Interprets False mouvement Inferred relationship Some 3
    Segmental cord myoclonus Interprets False mouvement Inferred relationship Some 2
    Palatal-tympanic myoclonus Interprets False mouvement Inferred relationship Some 2
    Hyoid myoclonus Interprets False mouvement Inferred relationship Some 2
    Opsoclonus-myoclonus syndrome Interprets False mouvement Inferred relationship Some 2
    A type of epilepsy that presents with myoclonic-atonic seizures usually between 2 to 6 years of age. Other generalised seizure types which may be seen in this syndrome include atonic, myoclonic, generalised tonic-clonic seizures, tonic and absence seizures. Nonconvulsive status epilepticus is common. Development prior to seizure onset is normal in two thirds of cases. These children typically show developmental stagnation or even regression during the active seizures (stormy) phase, which improves once seizures are controlled. The electroencephalogram shows generalised 2 to 6 Hz spike-wave or polyspike-and-wave abnormalities, with normal background. Interprets False mouvement Inferred relationship Some 2
    Unverricht-Lundborg syndrome Interprets False mouvement Inferred relationship Some 2
    Lafora disease Interprets False mouvement Inferred relationship Some 2
    A rare mitochondrial oxidative phosphorylation disorder characterized by myoclonic seizures, ataxia, generalized epilepsy, muscle weakness and ragged red fibers in the muscle biopsy. Interprets False mouvement Inferred relationship Some 4
    Sleep-related dystonia Interprets False mouvement Inferred relationship Some 2
    Cluster tic syndrome Interprets False mouvement Inferred relationship Some 2
    Painful legs and moving toes Interprets False mouvement Inferred relationship Some 4

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