255361000: Slow (qualifier value)

SNOMED CT Concept\Qualifier value (qualifier value)\...

\Descriptor (qualifier value)\Velocities\Slow

\Finding value (qualifier value)\Degree findings\Slow

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

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
Psychomotor retardation due to and following embolic cerebrovascular accident (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	2
Psychomotor retardation due to and following cerebrovascular accident with intracranial hemorrhage	Has interpretation	True	Slow	Inferred relationship	Some	2
Psychomotor retardation due to and following ischemic cerebrovascular accident	Has interpretation	True	Slow	Inferred relationship	Some	2
Stable bradyarrhythmia (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	1
Slow rate of urinary bladder filling	Has interpretation	True	Slow	Inferred relationship	Some	2
Slow weight gain (finding)	Has interpretation	True	Slow	Inferred relationship	Some	1
A rare parkinsonian syndrome due to neurodegenerative disease characterised by resting tremor (which may initially be asymmetric), rigidity, and bradykinesia. Polyneuropathy with neurogenic electromyography findings is present in the majority of the patients and reported in young age (early twenties) whereas parkinsonian symptoms are visible later in life (between 40 and 70 years of age). Additional clinical symptoms may include anxiety and depression. Mild diffuse muscular atrophy can also be detected in some patients.	Has interpretation	True	Slow	Inferred relationship	Some	2
Symptomatic parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Syphilitic parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Striatonigral degeneration	Has interpretation	True	Slow	Inferred relationship	Some	2
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	6
Impaired psychomotor performance (finding)	Has interpretation	True	Slow	Inferred relationship	Some	1
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	True	Slow	Inferred relationship	Some	5
Parkinsonism caused by carbon disulfide (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	2
Parkinsonism caused by methanol	Has interpretation	True	Slow	Inferred relationship	Some	2
X-linked dystonia parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Perry syndrome	Has interpretation	True	Slow	Inferred relationship	Some	2
Abrupt onset of dystonia with parkinsonism over a period of hours to days.	Has interpretation	True	Slow	Inferred relationship	Some	2
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	True	Slow	Inferred relationship	Some	4
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	True	Slow	Inferred relationship	Some	6
Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	4
Parkinsonism co-occurrent and due to acute infection (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	3
Parkinsonism due to human immunodeficiency virus infection (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	2
Parkinsonism following infection (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	3
Parkinsonism due to hereditary spastic paraplegia (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	3
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	True	Slow	Inferred relationship	Some	2
Parkinsonism due to heredodegenerative disorder (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	3
Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment.	Has interpretation	True	Slow	Inferred relationship	Some	2
Infection causing parkinsonism (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	2
Parkinsonism due to and following injury of head (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	4
Parkinsonism due to mass lesion of brain (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	3
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity.	Has interpretation	True	Slow	Inferred relationship	Some	2
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	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	True	Slow	Inferred relationship	Some	2
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	True	Slow	Inferred relationship	Some	3
Sporadic infantile bilateral striatal necrosis	Has interpretation	True	Slow	Inferred relationship	Some	2
Secondary parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Carbon monoxide-induced parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Manganese-induced parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Postencephalitic parkinsonism	Has interpretation	True	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	True	Slow	Inferred relationship	Some	3
Bradykinesia (finding)	Has interpretation	True	Slow	Inferred relationship	Some	1
Dissociative neurological symptom disorder co-occurrent with parkinsonism (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	2
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	True	Slow	Inferred relationship	Some	3
On - off phenomenon (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	2
Neuroleptic-induced parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	2
Parkinsonism following Mycoplasma infection (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	2
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	1
Amyotrophic lateral sclerosis with parkinsonism	Has interpretation	True	Slow	Inferred relationship	Some	1
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder)	Has interpretation	True	Slow	Inferred relationship	Some	1
Familial multiple system tauopathy	Has interpretation	True	Slow	Inferred relationship	Some	2
Frontotemporal dementia with parkinsonism-17	Has interpretation	True	Slow	Inferred relationship	Some	6

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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