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255361000: Slow (qualifier value)

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
380557015 Slow en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
646390015 Slow (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
102261000077118 lent fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Slow Is a Velocities true Inferred relationship Some
Slow Is a Degree findings true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Very slow Is a True Slow Inferred relationship Some
Baseline bradycardia Has interpretation False Slow Inferred relationship Some 1
Reflex bradycardia Has interpretation False Slow Inferred relationship Some 1
On examination - pulse rate - bradycardia Has interpretation False Slow Inferred relationship Some 2
Bradycardia - baseline fetal heart rate (finding) Has interpretation False Slow Inferred relationship Some 1
Bradycardia Has interpretation False Slow Inferred relationship Some 1
Bradycardia - baseline fetal heart rate (finding) Has interpretation False Slow Inferred relationship Some 1
On examination - pulse rate - bradycardia Has interpretation False Slow Inferred relationship Some 2
Baseline bradycardia Has interpretation True Slow Inferred relationship Some 1
Reflex bradycardia Has interpretation True Slow Inferred relationship Some 1
Bradycardia Has interpretation True Slow Inferred relationship Some 1
Vagal autonomic bradycardia of prematurity (disorder) Has interpretation True Slow Inferred relationship Some 1
Persistent sinus bradycardia (disorder) Has interpretation True Slow Inferred relationship Some 1
Sinus bradycardia Has interpretation True Slow Inferred relationship Some 1
Fetal bradycardia Has interpretation True Slow Inferred relationship Some 1
AV-junctional (nodal) bradycardia Has interpretation True Slow Inferred relationship Some 1
Vagal autonomic bradycardia Has interpretation True Slow Inferred relationship Some 1
Symptomatic sinus bradycardia (disorder) Has interpretation True Slow Inferred relationship Some 1
Supraventricular bradyarrhythmia Has interpretation True Slow Inferred relationship Some 1
Bradyarrhythmia (disorder) Has interpretation True Slow Inferred relationship Some 1
Neonatal bradycardia (disorder) Has interpretation True Slow Inferred relationship Some 1
Severe sinus bradycardia Has interpretation True Slow Inferred relationship Some 1
Tachycardia-bradycardia Has interpretation True Slow Inferred relationship Some 2
Fetal heart baseline rate range 40 to 80 (finding) Has interpretation True Slow Inferred relationship Some 2
Fetal heart baseline rate range 80 to 100 (finding) Has interpretation True Slow Inferred relationship Some 2
Bradycardia - baseline fetal heart rate (finding) Has interpretation True Slow Inferred relationship Some 2
Sinus bradycardia caused by drug (disorder) Has interpretation True Slow Inferred relationship Some 3
Sinus bradycardia due to metabolic disease Has interpretation True Slow Inferred relationship Some 5
Psychomotor retardation Has interpretation True Slow Inferred relationship Some 1
Parkinsonism Has interpretation False Slow Inferred relationship Some 3
A rare neurodegenerative disease usually presenting before the age of 30 and which is characterized by dystonia, L-dopa-responsive parkinsonism, pyramidal signs and rapid cognitive decline. Has interpretation False Slow Inferred relationship Some 4
Bradykinesia (finding) Has interpretation False Slow Inferred relationship Some 2
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder) Has interpretation False Slow Inferred relationship Some 7
Syphilitic parkinsonism Has interpretation False Slow Inferred relationship Some 3
Striatonigral degeneration Has interpretation False Slow Inferred relationship Some 3
Postencephalitic parkinsonism Has interpretation False Slow Inferred relationship Some 4
Juvenile Parkinson's disease Has interpretation True Slow Inferred relationship Some 3
Secondary parkinsonism Has interpretation False Slow Inferred relationship Some 3
Carbon monoxide-induced parkinsonism Has interpretation False Slow Inferred relationship Some 4
Manganese-induced parkinsonism Has interpretation False Slow Inferred relationship Some 4
Parkinsonism with calcification of basal ganglia Has interpretation True Slow Inferred relationship Some 3
Vascular parkinsonism Has interpretation True Slow Inferred relationship Some 3
Symptomatic parkinsonism Has interpretation False Slow Inferred relationship Some 3
On - off phenomenon (disorder) Has interpretation False Slow Inferred relationship Some 4
Impaired psychomotor performance (finding) Has interpretation False Slow 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. Has interpretation False Slow Inferred relationship Some 6
Parkinsonism caused by carbon disulfide (disorder) Has interpretation False Slow Inferred relationship Some 4
Parkinsonism caused by methanol Has interpretation False Slow Inferred relationship Some 4
X-linked dystonia parkinsonism Has interpretation False Slow Inferred relationship Some 3
Perry syndrome Has interpretation False Slow Inferred relationship Some 3
Abrupt onset of dystonia with parkinsonism over a period of hours to days. Has interpretation False Slow Inferred relationship Some 3
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. Has interpretation False Slow Inferred relationship Some 5
A rare parkinsonian syndrome due to intoxication which develops in individuals surviving an acute cyanide intoxication episode or due to chronic exposure to small cyanide doses. It presents several weeks after acute exposure with progressive typical clinical features of parkinsonism including bradykinesia, rigidity, dystonia, hypomimia, hypokinetic dysarthria, postural instability and retropulsion but no resting or postural tremor. Brain MRI reveals bilateral lesions in the pallidum, posterior putamen, substantia nigra, subthalamic nucleus, temporal and occipital cortex, and cerebellum. Has interpretation True Slow Inferred relationship Some 3
Dissociative neurological symptom disorder co-occurrent with parkinsonism (disorder) Has interpretation False Slow Inferred relationship Some 3
A rare neuronal ceroid lipofuscinosis disorder characterized by juvenile-onset of progressive spinocerebellar ataxia, bulbar syndrome (manifesting with dysarthria, dysphagia and dysphonia), pyramidal and extrapyramidal involvement (including myoclonus, amyotrophy, unsteady gait, akinesia, rigidity, dysarthric speech) and intellectual deterioration. Muscle biopsy displays autofluorescent bodies and lipofuscin deposits in brain and, occasionally the retina, upon postmortem. Has interpretation False Slow Inferred relationship Some 7
Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder) Has interpretation False Slow Inferred relationship Some 5
Parkinsonism co-occurrent and due to acute infection (disorder) Has interpretation False Slow Inferred relationship Some 4
Parkinsonism due to human immunodeficiency virus infection (disorder) Has interpretation False Slow Inferred relationship Some 3
Parkinsonism following infection (disorder) Has interpretation False Slow Inferred relationship Some 4
Parkinsonism due to hereditary spastic paraplegia (disorder) Has interpretation False Slow Inferred relationship Some 4
Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal. Has interpretation False Slow Inferred relationship Some 3
Atypical Parkinsonism (disorder) Has interpretation True Slow Inferred relationship Some 3
Parkinsonism due to heredodegenerative disorder (disorder) Has interpretation False Slow Inferred relationship Some 4
Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment. Has interpretation False Slow Inferred relationship Some 3
Infection causing parkinsonism (disorder) Has interpretation False Slow Inferred relationship Some 3
Sporadic Parkinson disease (disorder) Has interpretation True Slow Inferred relationship Some 3
Parkinsonism due to and following injury of head (disorder) Has interpretation False Slow Inferred relationship Some 5
Parkinsonism due to mass lesion of brain (disorder) Has interpretation False Slow Inferred relationship Some 4
Functional parkinsonism (disorder) Has interpretation True Slow Inferred relationship Some 2
A complex form of young-onset Parkinson disease that manifests with pyramidal signs, eye movement abnormalities, psychiatric manifestations (depression, anxiety, drug-induced psychosis, and impulse control disorders), intellectual disability, and other neurological symptoms (such as ataxia and epilepsy) along with classical parkinsonian symptoms. Has interpretation True Slow Inferred relationship Some 3
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Has interpretation False Slow Inferred relationship Some 3
A rare, genetic, parkinsonian disorder characterized by an age of onset between 21-45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints and falls, and other non-motor symptoms. A slow disease progression and a more pronounced response to dopaminergic therapy are also observed in most forms of this disease. Has interpretation True Slow Inferred relationship Some 3
Parkinsonism with dementia of Guadeloupe is characterized by symmetrical bradykinesia, predominantly axial rigidity, postural instability with early falls and cognitive decline with prominent features of frontal lobe dysfunction. Has interpretation False Slow Inferred relationship Some 4
A rare X-linked syndromic intellectual disability characterized by infantile-onset non-progressive intellectual deficit (with psychomotor developmental delay, cognitive impairment and macrocephaly) and early-onset parkinsonism (before 45 years of age), in male patients. Has interpretation True Slow Inferred relationship Some 4
Hereditary late-onset Parkinson disease (LOPD) is a form of Parkinson disease (PD), characterized by an age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia (LID). Has interpretation True Slow Inferred relationship Some 3
Infantile bilateral striatal necrosis (IBSN) comprises several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic. Has interpretation False Slow Inferred relationship Some 3
Hemiparkinsonism-hemiatrophy syndrome is a rare parkinsonian disorder characterized by unilateral body atrophy and slowly progressive, ipsilateral, hemiparkinsonian signs (bradykinesia, rigidity, and tremor). Patients typically present with unilateral, action-induced dystonia, in upper or lower limbs, that progresses and becomes bilateral or with tremor which occurs predominantly at rest and progresses to hemiparkinsonism. Scoliosis, scapular winging, raised shoulders, brisk reflexes and extensor plantar responses are frequently associated. Has interpretation False Slow Inferred relationship Some 4
Parkinsonian-pyramidal syndrome is a rare, genetic, neurological disorder characterized by the association of both parkinsonian (i.e. bradykinesia, rigidity and/or rest tremor) and pyramidal (i.e. increased reflexes, extensor plantar reflexes, pyramidal weakness or spasticity) manifestations, which vary according to the underlying associated disease (e.g. neurodegenerative disease, inborn errors of metabolism). Has interpretation False Slow Inferred relationship Some 4
Sporadic infantile bilateral striatal necrosis Has interpretation False Slow Inferred relationship Some 3
Autosomal recessive familial Parkinson disease Has interpretation True Slow Inferred relationship Some 3
Progressive supranuclear palsy parkinsonism syndrome (disorder) Has interpretation True Slow Inferred relationship Some 6
Neuroleptic-induced parkinsonism Has interpretation False Slow Inferred relationship Some 3
Parkinson's disease Has interpretation True Slow Inferred relationship Some 2
MPTP-induced parkinsonism Has interpretation True Slow Inferred relationship Some 2
Parkinsonism caused by drug Has interpretation True Slow Inferred relationship Some 2
Psychosis co-occurrent and due to Parkinson's disease (disorder) Has interpretation True Slow Inferred relationship Some 2
Parkinsonism following Mycoplasma infection (disorder) Has interpretation False Slow Inferred relationship Some 3
Parkinsonism due to prion disease (disorder) Has interpretation True Slow Inferred relationship Some 3
Toxin-induced parkinsonism Has interpretation True Slow Inferred relationship Some 2
Parkinsonism caused by pesticide (disorder) Has interpretation True Slow Inferred relationship Some 2
Familial infantile bilateral striatal necrosis is the familial form of infantile bilateral striatal necrosis, a syndrome of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. Has interpretation True Slow Inferred relationship Some 2
Asymptomatic bradycardia Has interpretation True Slow Inferred relationship Some 1
A rare neurologic disease characterized by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction. Has interpretation True Slow Inferred relationship Some 3
Drug-induced bradycardia (disorder) Has interpretation True Slow Inferred relationship Some 1
A rare clinical situation occurring in the context of Parkinson disease characterized by return or worsening of symptoms (including motor and/or non-motor symptoms) under antiparkinsonian therapy. Types of off-periods are Morning Off (experienced before the first dose of the day), Delayed On (occurring more frequently after the first dose of the day or after meals), Wearing Off (end-of-dose deterioration), Sudden Off (sudden transition from on to off), and Dose Failure. Has interpretation True Slow Inferred relationship Some 2
Amyotrophic lateral sclerosis with parkinsonism Has interpretation False Slow Inferred relationship Some 3
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder) Has interpretation False Slow Inferred relationship Some 5
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder) Has interpretation False Slow Inferred relationship Some 5
Parkinsonism caused by dopamine receptor antagonist (disorder) Has interpretation True Slow Inferred relationship Some 2
Parkinsonism caused by dopamine depleting agent (disorder) Has interpretation True Slow Inferred relationship Some 2
Psychomotor retardation due to and following embolic cerebrovascular accident (disorder) Has interpretation True Slow Inferred relationship Some 2

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