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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
Postural tremor of upper limb (finding) Interprets True Movement observable Inferred relationship Some 2
Tremor of limb (finding) Interprets True Movement observable Inferred relationship Some 2
Trismus following procedure on tooth Interprets True Movement observable Inferred relationship Some 4
Postencephalitic myoclonus Interprets True Movement observable Inferred relationship Some 2
Tremor due to harmful pattern of substance use Interprets True Movement observable Inferred relationship Some 2
Contracture of muscle following injury Interprets True Movement observable Inferred relationship Some 3
Movement disorder due to toxicity of substance Interprets True Movement observable Inferred relationship Some 3
Hyperextension injury of neck Interprets True Movement observable Inferred relationship Some 3
Idiopathic orofacial dystonia Interprets True Movement observable Inferred relationship Some 3
Edentulous orofacial dystonia Interprets True Movement observable Inferred relationship Some 4
Drug-induced dyskinesia Interprets True Movement observable Inferred relationship Some 2
Tremor due to pheochromocytoma Interprets True Movement observable Inferred relationship Some 2
Autosomal recessive familial Parkinson disease Interprets True Movement observable Inferred relationship Some 3
Progressive supranuclear palsy parkinsonism syndrome (disorder) Interprets True Movement observable Inferred relationship Some 6
Idiopathic familial dystonia Interprets True Movement observable Inferred relationship Some 2
Idiopathic torsion dystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
A rare genetic dystonia characterized by focal or segmental isolated dystonia involving the face, neck, upper limbs (commonly writing dystonia), larynx, or trunk, with an onset from childhood to early adulthood. Dystonia may be tremulous, giving rise to head or hand tremor. Mode of inheritance is autosomal recessive. Interprets True Movement observable Inferred relationship Some 2
A rare neurologic disease characterized by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction. Interprets True Movement observable Inferred relationship Some 3
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. Interprets True Movement observable Inferred relationship Some 2
Myoclonus due to paraneoplastic syndrome (disorder) Interprets True Movement observable Inferred relationship Some 2
Optic ataxia Interprets True Movement observable Inferred relationship Some 2
Paraneoplastic opsoclonus myoclonus syndrome Interprets True Movement observable Inferred relationship Some 2
Oculomotor nerve synkinesis Interprets True Movement observable Inferred relationship Some 1
A rare genetic epilepsy syndrome characterized by infantile or childhood onset of focal motor seizures remitting with age, as well as childhood onset of exercise-induced dystonia which often persists into adulthood. Additional reported features include nystagmus and postural tremor of the hands. Interprets True Movement observable Inferred relationship Some 3
Psychogenic tremor (disorder) Interprets True Movement observable Inferred relationship Some 1
Neuroleptic-induced tardive dyskinesia Interprets True Movement observable Inferred relationship Some 1
A rare genetic neurological disorder characterized by childhood-onset dystonia with distinctive MRI changes in the basal ganglia, and optic atrophy developing either immediately or within a few years after the appearance of dystonia. Additional symptoms include chorea and other movement disorders, dysarthria, or nystagmus, among others. Motor disability progresses gradually, while cognitive function is relatively spared. Interprets True Movement observable Inferred relationship Some 3
Finding of movement Interprets True Movement observable Inferred relationship Some 1
Movement disorder Interprets True Movement observable Inferred relationship Some 1
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 True Movement observable Inferred relationship Some 3
Tremor due to substance withdrawal (finding) Interprets True Movement observable Inferred relationship Some 2
Aspergillus clavatus tremors Interprets True Movement observable Inferred relationship Some 3
Impairment of motor nerve function as a complication of cutaneous surgery Interprets True Movement observable Inferred relationship Some 3
Amyotrophic lateral sclerosis with parkinsonism Interprets True Movement observable Inferred relationship Some 1
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder) Interprets True Movement observable Inferred relationship Some 1
Bobble-head doll syndrome Interprets True Movement observable Inferred relationship Some 1
Ataxia due to subpial siderosis (disorder) Interprets True Movement observable Inferred relationship Some 2
Acquired ataxia due to vitamin deficiency Interprets True Movement observable Inferred relationship Some 2
A rare, genetic, neurological disorder characterized by childhood-onset severe myoclonic and tonic-clonic seizures and early-onset ataxia leading to severe gait disturbances associated with normal to slightly diminished cognition. Scoliosis, diffuse muscle atrophy and subcutaneous fat loss, as well as developmental delay, may be associated. Brain MRI may reveal complete agenesis of the corpus callosum, ventriculomegaly, interhemispheric cysts, and simplified gyration (frontally). Interprets True Movement observable Inferred relationship Some 3
A rare persistent combined dystonia characterized by childhood onset of progressive dystonia typically beginning in the lower limbs and eventually progressing to generalized dystonia with involvement of the upper limbs, trunk, face, and neck. Variable developmental delay and intellectual disability, as well as mild microcephaly, short stature, abnormal eye movements, and slightly dysmorphic facial features have been reported in association. Interprets True Movement observable Inferred relationship Some 3
Insomnia due to periodic limb movement disorder (disorder) Interprets True Movement observable Inferred relationship Some 2
Dissociative neurological disorder with symptom of movement disorder (disorder) Interprets True Movement observable Inferred relationship Some 1
Dissociative neurological symptom disorder co-occurrent with dystonia (disorder) Interprets True Movement observable Inferred relationship Some 2
Dissociative neurological symptom disorder co-occurrent with myoclonus (disorder) Interprets True Movement observable Inferred relationship Some 2
A rare genetic neurological disorder with characteristics of childhood onset of severe global neurodevelopmental regression with eventual loss of independent walking and loss of language and fine and gross motor skills, and development of severe dysphagia requiring tube feeding, seizures, cerebellar syndrome, dystonia, and other neurologic manifestations. Brain imaging shows progressive cerebral and/or cerebellar atrophy in most cases. A less severe phenotype associated with missense mutations shows no regression or movement abnormalities, ambulation is preserved, and brain imaging is normal. Interprets True Movement observable Inferred relationship Some 4
Late onset dementia due to Lewy body disease Interprets True Movement observable Inferred relationship Some 5
Dementia due to Lewy body disease Interprets True Movement observable Inferred relationship Some 5
Early onset dementia due to Lewy body disease (disorder) Interprets True Movement observable Inferred relationship Some 5
Lewy body dementia with behavioral disturbance Interprets True Movement observable Inferred relationship Some 5
Acute mastoiditis with facial paralysis Interprets True Movement observable Inferred relationship Some 2
Cranial nerve palsy due to type 1 diabetes mellitus Interprets True Movement observable Inferred relationship Some 2
Cranial nerve palsy due to type 2 diabetes mellitus Interprets True Movement observable Inferred relationship Some 2
Cranial nerve palsy due to diabetes mellitus Interprets True Movement observable Inferred relationship Some 2
Nerve palsy Interprets True Movement observable Inferred relationship Some 1
A rare, localized variant of Guillain-Barré syndrome characterized by rapidly progressive bilateral facial nerve palsy, distal paresthesias, and minimal or no motor weakness. Deep tendon reflexes are usually diminished or absent but can be present or even exaggerated in rare cases. CSF analysis may reveal albuminocytologic dissociation. Nerve conduction velocity studies often show demyelinating type of neuropathy, although axonal polyneuropathy has been also described. Interprets True Movement observable Inferred relationship Some 3
A rare peripheral neuropathy characterized by an acute onset of unilateral facial muscle weakness with Bell's phenomenon. It is non-progressive, resolves spontaneously, and it might be recurrent with no obvious precipitating factors. Interprets True Movement observable Inferred relationship Some 1
A very rare congenital cranial dysinnervation disorder characterised by unilateral or bilateral non progressive congenital facial palsy (VII cranial nerve) with impairments of ocular abduction (VI cranial nerve). It can also be associated with other cranial nerves palsies, orofacial anomalies and limb defects. Interprets True Movement observable Inferred relationship Some 1
Paralysis of cervical sympathetic trunk (disorder) Interprets True Movement observable Inferred relationship Some 2
Vagus nerve laryngeal paralysis Interprets True Movement observable Inferred relationship Some 1
Ptosis-vocal cord paralysis syndrome is a rare, hereditary disorder with ptosis characterized by the combination of congenital bilateral recurrent laryngeal nerve paralysis and congenital bilateral ptosis. There have been no further descriptions in the literature since 1983. Interprets True Movement observable Inferred relationship Some 1
Frontotemporal dementia with parkinsonism-17 Interprets True Movement observable Inferred relationship Some 6
Stiff neck symptom (finding) Interprets True Movement observable Inferred relationship Some 1
Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to iron responsive element binding protein 2 gene mutation (disorder) Interprets True Movement observable Inferred relationship Some 2

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