255324009: Movement (observable entity)

SNOMED CT Concept\Observable entity\Process (observable entity)\Movement

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Movement	Is a	Gross motor functions	false	Inferred relationship	Some
Movement	Is a	Process (observable entity)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
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	Inferred relationship	Some	3
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	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	Inferred relationship	Some	2
A rare lethal multiple congenital anomalies/dysmorphic syndrome characterized by the association of fetal akinesia sequence, bilateral microphthalmia, microtia, and persistent truncus arteriosus. Additional dysmorphic features include prominent forehead, small nose, micrognathia, as well as camptodactyly and symphalangism. Contractures of large joints and micropenis have also been reported.	Interprets	False	Movement	Inferred relationship	Some	6
Myoclonus due to paraneoplastic syndrome (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
Optic ataxia	Interprets	True	Movement	Inferred relationship	Some	2
Paraneoplastic opsoclonus myoclonus syndrome	Interprets	True	Movement	Inferred relationship	Some	2
Oculomotor nerve synkinesis	Interprets	True	Movement	Inferred relationship	Some	3
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	Inferred relationship	Some	3
Paralysis of diaphragm	Interprets	True	Movement	Inferred relationship	Some	3
Relaxation of diaphragm	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis due to lesion of spinal cord (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Epidural ascending spinal paralysis	Interprets	True	Movement	Inferred relationship	Some	3
Spinal paraplegia	Interprets	True	Movement	Inferred relationship	Some	4
Acute atrophic spinal paralysis	Interprets	True	Movement	Inferred relationship	Some	3
Quadriplegic spinal paralysis (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Acute complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra	Interprets	True	Movement	Inferred relationship	Some	5
Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Acute complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra	Interprets	True	Movement	Inferred relationship	Some	5
Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder)	Interprets	True	Movement	Inferred relationship	Some	5
Chronic paralysis due to lesion of spinal cord	Interprets	True	Movement	Inferred relationship	Some	4
Acute paralysis due to lesion of spinal cord (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Spastic spinal syphilitic paralysis	Interprets	True	Movement	Inferred relationship	Some	4
Paralysis of tongue	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis of left side of tongue	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis of right side of tongue (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Bilateral paralysis of tongue	Interprets	True	Movement	Inferred relationship	Some	4
Paralysis of palate (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis of uvula	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis of uvula after diphtheria (disorder)	Interprets	True	Movement	Inferred relationship	Some	5
Paralytic syndrome of bilateral lower limbs (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Tetraplegia	Interprets	True	Movement	Inferred relationship	Some	3
Painful ophthalmoplegia	Interprets	True	Movement	Inferred relationship	Some	4
Krydset hemiplegi	Interprets	False	Movement	Inferred relationship	Some	3
Ophthalmoplegia plus syndrome	Interprets	True	Movement	Inferred relationship	Some	4
Total ophthalmoplegia	Interprets	True	Movement	Inferred relationship	Some	3
A disorder of the superior trunk of the brachial plexus or the fifth and sixth cervical spinal nerves or motor roots, resulting in weakness of proximal upper extremity musculature innervated by these nerve roots	Interprets	True	Movement	Inferred relationship	Some	4
Monoparesis	Interprets	True	Movement	Inferred relationship	Some	3
Spastic hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Supranuclear paralysis	Interprets	True	Movement	Inferred relationship	Some	3
Cerebral paresis with homolateral ataxia	Interprets	True	Movement	Inferred relationship	Some	3
Alternating hypoglossal hemiplegia	Interprets	True	Movement	Inferred relationship	Some	4
Paraplegia	Interprets	True	Movement	Inferred relationship	Some	4
Acute paralytic poliomyelitis, bulbar	Interprets	True	Movement	Inferred relationship	Some	4
Monoplegia	Interprets	True	Movement	Inferred relationship	Some	3
Cerebral paraparesis	Interprets	True	Movement	Inferred relationship	Some	4
Spinal hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Cerebral paralysis with homolateral ataxia	Interprets	True	Movement	Inferred relationship	Some	3
Monoplegia of lower limb	Interprets	True	Movement	Inferred relationship	Some	3
Flaccid hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Klumpke-Déjerine paralysis	Interprets	True	Movement	Inferred relationship	Some	3
Transient hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Chronic progressive paraparesis	Interprets	True	Movement	Inferred relationship	Some	4
An ophthalmoplegic syndrome, affecting all age groups, with characteristics of acute attacks (lasting a few days to a few weeks) of periorbital pain, ipsilateral ocular motor nerve palsies, ptosis, disordered eye movements and blurred vision usually caused by a non-specific inflammatory process in the cavernous sinus and superior orbital fissure. It has an unpredictable course with spontaneous remission occurring in some and recurrence of attacks in others.	Interprets	True	Movement	Inferred relationship	Some	3
Hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Diplegia of upper limbs	Interprets	True	Movement	Inferred relationship	Some	3
Partial bilateral paralysis	Interprets	True	Movement	Inferred relationship	Some	3
Parinaud's syndrome	Interprets	True	Movement	Inferred relationship	Some	4
Locked in syndrome	Interprets	True	Movement	Inferred relationship	Some	3
Facial hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Cerebral hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Monoplegia of upper limb	Interprets	True	Movement	Inferred relationship	Some	3
Spastic tetraplegia with rigidity syndrome	Interprets	True	Movement	Inferred relationship	Some	4
Progressive supranuclear ophthalmoplegia	Interprets	True	Movement	Inferred relationship	Some	3
Crossed hemiparesis	Interprets	True	Movement	Inferred relationship	Some	3
Complete bilateral paralysis	Interprets	True	Movement	Inferred relationship	Some	3
Paralytic syndrome	Interprets	True	Movement	Inferred relationship	Some	2
Triparesis	Interprets	True	Movement	Inferred relationship	Some	3
Cerebral paraplegia	Interprets	True	Movement	Inferred relationship	Some	4
Recurrent painful ophthalmoplegic neuropathy	Interprets	True	Movement	Inferred relationship	Some	4
Internuclear ophthalmoplegia	Interprets	True	Movement	Inferred relationship	Some	4
Ophthalmoplegia	Interprets	True	Movement	Inferred relationship	Some	4
Facial hemiparesis	Interprets	True	Movement	Inferred relationship	Some	3
Hemiparesis	Interprets	True	Movement	Inferred relationship	Some	3
Diplegia	Interprets	True	Movement	Inferred relationship	Some	3
Triplegia	Interprets	True	Movement	Inferred relationship	Some	3
Palsy of conjugate gaze	Interprets	True	Movement	Inferred relationship	Some	4
Infantile hemiplegia	Interprets	True	Movement	Inferred relationship	Some	3
Cerebral hemiparesis	Interprets	True	Movement	Inferred relationship	Some	3
Paraparesis	Interprets	True	Movement	Inferred relationship	Some	4
Spasm of conjugate gaze	Interprets	True	Movement	Inferred relationship	Some	3
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain.	Interprets	True	Movement	Inferred relationship	Some	4
Paralysis of vagus, spinal accessory and hypoglossal nerves	Interprets	True	Movement	Inferred relationship	Some	3
Paralytisk apopleksi	Interprets	True	Movement	Inferred relationship	Some	4
Flaccid tetraplegia	Interprets	True	Movement	Inferred relationship	Some	3
Spastic tetraplegia	Interprets	True	Movement	Inferred relationship	Some	4
Flaccid paraplegia (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Spastic paraplegia	Interprets	True	Movement	Inferred relationship	Some	4
Acute paralytic non-bulbar poliomyelitis	Interprets	True	Movement	Inferred relationship	Some	4
Acute paralytic poliomyelitis, wild virus, imported	Interprets	True	Movement	Inferred relationship	Some	4
Acute paralytic poliomyelitis, wild virus, indigenous	Interprets	True	Movement	Inferred relationship	Some	4
Pure hereditary spastic paraplegia (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Complicated hereditary spastic paraplegia	Interprets	True	Movement	Inferred relationship	Some	4
A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense.	Interprets	True	Movement	Inferred relationship	Some	8
Alternating hemiplegia of childhood	Interprets	True	Movement	Inferred relationship	Some	4
Congenital nuclear ophthalmoplegia	Interprets	True	Movement	Inferred relationship	Some	4
A type of cerebral palsy defined by increased tone and pathological reflexes resulting in an abnormal pattern of movement and posture.	Interprets	True	Movement	Inferred relationship	Some	4

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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
2235911000005118	Bevægelse	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)