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363847004: Movement observable (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
486976015 Movement observable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
770030010 Movement observable (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
168701000077111 entité observable du mouvement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

345 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Movement observable Is a Neurological observable (observable entity) false Inferred relationship Some
Movement observable Is a Observable entity (observable entity) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Reversed peristalsis Interprets True Movement observable Inferred relationship Some 4
Juvenile cerebellar degeneration AND myoclonus Interprets True Movement observable Inferred relationship Some 3
Atypical tic disorder Interprets True Movement observable Inferred relationship Some 2
Extrapyramidal disease Interprets True Movement observable Inferred relationship Some 2
Adductor spastic dysphonia of conversion reaction Interprets True Movement observable Inferred relationship Some 4
Opticocochleodentate degeneration Interprets True Movement observable Inferred relationship Some 2
Coarse tremor Interprets True Movement observable Inferred relationship Some 1
Flail elbow Interprets True Movement observable Inferred relationship Some 2
Diffuse Lewy body disease (disorder) Interprets True Movement observable Inferred relationship Some 4
Hemiballism Interprets True Movement observable Inferred relationship Some 2
Tremor opiophagorum Interprets True Movement observable Inferred relationship Some 1
Ambulatory automatism Interprets True Movement observable Inferred relationship Some 1
Familial essential myoclonus Interprets True Movement observable Inferred relationship Some 2
Musculoskeletal immobility Interprets True Movement observable Inferred relationship Some 3
Olivopontocerebellar degeneration Interprets True Movement observable Inferred relationship Some 2
Finding of movement of thorax Interprets True Movement observable Inferred relationship Some 2
Extrapyramidal movements (finding) Interprets True Movement observable Inferred relationship Some 1
Habit tic (disorder) Interprets True Movement observable Inferred relationship Some 3
Recurrent transient tic disorder Interprets True Movement observable Inferred relationship Some 4
Movements used to potentiate, accentuate, or compensate for an impairment in a physiologic motion (e.g., the movements needed to move a paralyzed limb). Interprets True Movement observable Inferred relationship Some 3
Impaired psychomotor performance (finding) Interprets True Movement observable Inferred relationship Some 1
Anterior sacral nutation (finding) Interprets True Movement observable Inferred relationship Some 2
Translatory motion (observable entity) Is a True Movement observable Inferred relationship Some
Bilateral sacral extension (finding) Interprets True Movement observable Inferred relationship Some 3
Sacral nutation (finding) Interprets True Movement observable Inferred relationship Some 2
Changes in position of body structures within the normal range. Is a True Movement observable Inferred relationship Some
Bilateral sacral flexion (finding) Interprets True Movement observable Inferred relationship Some 2
Posterior movement of the base of the sacrum in relation to the ilia. Interprets True Movement observable Inferred relationship Some 2
Sacral flexion (finding) Interprets True Movement observable Inferred relationship Some 1
Medication-induced movement disorder Interprets True Movement observable Inferred relationship Some 3
Drug-induced dystonia Interprets True Movement observable Inferred relationship Some 3
Drug-induced orofacial dyskinesia (disorder) Interprets True Movement observable Inferred relationship Some 3
Abdominal movement diminished (finding) Interprets True Movement observable Inferred relationship Some 2
Abdominal wall movement (finding) Interprets True Movement observable Inferred relationship Some 2
Periodic limb movement disorder (disorder) Interprets True Movement observable Inferred relationship Some 1
Paradoxical inward movement of abdomen on inspiration (finding) Interprets True Movement observable Inferred relationship Some 2
Benign neonatal sleep myoclonus (disorder) Interprets True Movement observable Inferred relationship Some 3
Transient tic disorder Interprets True Movement observable Inferred relationship Some 3
Myoclonus of tensor tympani muscle (disorder) Interprets True Movement observable Inferred relationship Some 3
Segmental dystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
Apraxia due to cerebrovascular accident (disorder) Interprets True Movement observable Inferred relationship Some 2
Decreased peristalsis Interprets True Movement observable Inferred relationship Some 4
Difficulty controlling posture Interprets True Movement observable Inferred relationship Some 2
Unable to control head posture Interprets True Movement observable Inferred relationship Some 2
Difficulty controlling head posture Interprets True Movement observable Inferred relationship Some 2
Unable to control shoulder girdle posture Interprets True Movement observable Inferred relationship Some 2
Difficulty controlling shoulder girdle posture Interprets True Movement observable Inferred relationship Some 2
Unable to control trunk posture Interprets True Movement observable Inferred relationship Some 2
Difficulty controlling trunk posture Interprets True Movement observable Inferred relationship Some 2
Unable to control pelvic posture Interprets True Movement observable Inferred relationship Some 2
Difficulty controlling pelvic posture Interprets True Movement observable Inferred relationship Some 2
Unable to control posture Interprets True Movement observable Inferred relationship Some 2
No toe movement Interprets True Movement observable Inferred relationship Some 1
Orthostatic tremor (finding) Interprets True Movement observable Inferred relationship Some 1
Torsion dystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
Tremor in bilateral outstretched hands (finding) Interprets True Movement observable Inferred relationship Some 3
Tremor of tongue Interprets True Movement observable Inferred relationship Some 2
A rare neurodegenerative disease characterized by extrapyramidal symptoms (rigidity, tremor, bradykinesia) and dementia, typically beginning in the fifth or sixth decade of life and progressing to a vegetative state with pelvicrural flexion contractures within few years. Oculomotor signs, olfactory dysfunction, and autonomic disturbances may also be observed. Neuropathological hallmarks are frontotemporally accentuated cerebral atrophy, as well as neurofibrillary tangles and neuronal loss in a characteristic distribution in cortical and subcortical regions. The disease is endemic to the Pacific Island of Guam. Interprets True Movement observable Inferred relationship Some 5
Autoimmune opsoclonus myoclonus Interprets True Movement observable Inferred relationship Some 3
Acquired ataxia Interprets True Movement observable Inferred relationship Some 2
Ataxia due to chronic infection of central nervous system (disorder) Interprets True Movement observable Inferred relationship Some 3
Toxic dystonia Interprets True Movement observable Inferred relationship Some 2
Parkinsonism caused by carbon disulfide (disorder) Interprets True Movement observable Inferred relationship Some 2
Parkinsonism caused by methanol Interprets True Movement observable Inferred relationship Some 2
Essential tremor Interprets True Movement observable Inferred relationship Some 2
Laryngeal dystonia Interprets True Movement observable Inferred relationship Some 3
Organic sleep related movement disorder (disorder) Interprets True Movement observable Inferred relationship Some 2
Subacute dyskinesia caused by drug Interprets True Movement observable Inferred relationship Some 1
X-linked dystonia parkinsonism Interprets True Movement observable Inferred relationship Some 2
Brainstem myoclonus Interprets True Movement observable Inferred relationship Some 2
Cerebral cortex myoclonus (disorder) Interprets True Movement observable Inferred relationship Some 2
Spinal cord myoclonus Interprets True Movement observable Inferred relationship Some 2
Perry syndrome Interprets True Movement observable Inferred relationship Some 2
Focal motor weakness Interprets True Movement observable Inferred relationship Some 1
Autosomal recessive idiopathic familial dystonia Interprets True Movement observable Inferred relationship Some 2
Stiffness Interprets True Movement observable Inferred relationship Some 1
Congenital athetosis Interprets True Movement observable Inferred relationship Some 2
Abrupt onset of dystonia with parkinsonism over a period of hours to days. Interprets True Movement observable Inferred relationship Some 2
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis Interprets True Movement observable Inferred relationship Some 2
Deafness-dystonia-optic neuronopathy syndrome (disorder) Interprets True Movement observable Inferred relationship Some 4
Dystonia 6 Interprets True Movement observable Inferred relationship Some 2
Blepharospasm Interprets True Movement observable Inferred relationship Some 3
Tick paralysis Interprets True Movement observable Inferred relationship Some 3
Proximal myopathy with extrapyramidal signs is a rare, hereditary non-dystrophic myopathy characterized by proximal muscle weakness, delayed motor development, learning difficulties, and progressive extrapyramidal motor signs including chorea, dystonia and tremor. Variable additional features have been reported - ataxia, microcephaly, ophthalmoplegia, ptosis, and optic atrophy. Interprets True Movement observable Inferred relationship Some 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 observable Inferred relationship Some 5
A rare, genetic, neurological disorder characterized by parkinsonian features (including resting or action tremor, cogwheel rigidity, hypomimia and bradykinesia) associated with variably penetrant spasticity, hyperactive deep tendon reflexes and Babinski sign. Interprets True Movement observable Inferred relationship Some 4
A rare monogenic disease with epilepsy characterized by developmental delay and infantile spasms in the first months of life, followed by chorea and generalized dystonia and progressing to quadriplegic dyskinesia, recurrent status dystonicus, intractable focal epilepsy and severe intellectual disability. Interprets True Movement observable Inferred relationship Some 3
Acquired torsion dystonia (disorder) Interprets True Movement observable Inferred relationship Some 3
A rare, genetic, persistent combined dystonia characterized by clinical signs similar to ataxia-telangiectasia but with a later (usually adulthood) onset and slower progression. Patients typically present extrapyramidal signs, such as resting tremor, choreoathetosis, and dystonia, as the initial symptoms and later often develop mild cerebellar ataxia (with gait usually preserved). Telangiectasia and immunodeficiency may be absent but secondary features of ataxia-telangiectasia, such as risk of malignancy, dysarthria and peripheral neuropathy, are frequently present. Interprets True Movement observable Inferred relationship Some 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 observable Inferred relationship Some 2
Progressive myoclonic epilepsy with dystonia is a rare, genetic epilepsy syndrome characterized by neonatal or early infantile onset of severe, progressive, typically frequent and prolonged myoclonic seizures that are refractory to treatment, associated with localized and/or generalized paroxysmal dystonia (which later becomes persistent). Other features include severe hypotonia, hemiplegia, psychomotor regression (or lack of psychomotor development) and progressive cerebral and cerebellar atrophy, with affected individuals becoming progressively non-reactive to environmental stimuli. Interprets True Movement observable Inferred relationship Some 3
Familial dyskinesia and facial myokymia is a rare paroxysmal movement disorder, with childhood or adolescent onset, characterized by paroxysmal choreiform, dystonic, and myoclonic movements involving the limbs (mostly distal upper limbs), neck and/or face, which can progressively increase in both frequency and severity until they become nearly constant. Patients may also present with delayed motor milestones, perioral and periorbital dyskinesias, dysarthria, hypotonia, and weakness. Interprets True Movement observable Inferred relationship Some 3
Familial cortical myoclonus is a rare, genetic movement disorder characterized by autosomal dominant, adult-onset, slowly progressive, multifocal, cortical myoclonus. Patients present somatosensory-evoked, brief, jerky, involuntary movements in the face, arms and legs, associated in most cases with sustained, multiple, sudden falls without loss of consciousness. Seizures or other neurological deficits, aside from mild cerebellar ataxia late in the course of the illness, are absent. Interprets True Movement observable Inferred relationship Some 2
Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. Interprets True Movement observable Inferred relationship Some 3
An inherited disorder characterised by hypermanganesemia. Manganese accumulates in the region of the brain responsible for the coordination of movement causing dystonia and other uncontrolled movements. Two types of hypermanganesemia with dystonia have been identified; hypermanganesemia with dystonia, polycythaemia, and cirrhosis (HMDPC) and hypermanganesemia with dystonia 2 and they are distinguished by genetic cause and features. Inherited in an autosomal recessive pattern. Interprets True Movement observable Inferred relationship Some 2
A rare disorder of manganese transport characterized by progressive movement disorder and elevated blood manganese levels. Patients present in infancy or early childhood with loss of motor milestones, rapidly progressive dystonia, spasticity, bulbar dysfunction, and parkinsonism, resulting in loss of independent ambulation. Cognition may be impaired but is generally better preserved than motor function. Additional manifestations include abnormal head growth and skull deformities. Brain MRI shows abnormalities of the basal ganglia, variably also of other brain regions. Interprets True Movement observable Inferred relationship Some 2
Finding of movement of neck Interprets True Movement observable Inferred relationship Some 2
Nail dystrophy due to habit tic (disorder) Interprets True Movement observable Inferred relationship Some 3
Hereditary essential tremor Interprets True Movement observable Inferred relationship Some 2
Propriospinal myoclonus at sleep onset Interprets True Movement observable Inferred relationship Some 2
Sleep-related movement disorder caused by drug Interprets True Movement observable Inferred relationship Some 3

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