255324009: Movement (observable entity)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. Module: SNOMED CT core

Descriptions:

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

42051000077112 mouvement 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
mouvement	Is a	Gross motor functions (observable entity)	false	Inferred relationship	Some
mouvement	Is a	Process (observable entity)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Monoplegia of upper limb due to and following ischemic cerebrovascular accident (disorder)	Interprets	False	mouvement	Inferred relationship	Some	6
Hemiplegia of nondominant side due to and following embolic cerebrovascular accident (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Paraplegia due to and following cerebrovascular accident (disorder)	Interprets	False	mouvement	Inferred relationship	Some	6
Acute paralytic poliomyelitis, vaccine-associated	Interprets	False	mouvement	Inferred relationship	Some	5
Acute bulbar poliomyelitis caused by Human poliovirus 2	Interprets	False	mouvement	Inferred relationship	Some	4
Acute bulbar poliomyelitis caused by Human poliovirus 1	Interprets	False	mouvement	Inferred relationship	Some	4
Acute paralytic poliomyelitis caused by Human poliovirus 1 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Acute paralytic poliomyelitis caused by Human poliovirus 2	Interprets	False	mouvement	Inferred relationship	Some	4
Acute paralytic poliomyelitis caused by Human poliovirus 3 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Congenital fibrosis of inferior rectus muscle (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
A rare complex hereditary spastic paraplegia characterized by an early onset hypotonia that progresses to spasticity, global developmental delay, severe intellectual disability and speech impairment, microcephaly, short stature and dysmorphic features. Patients often become non-ambulatory, and some develop seizures and stereotypic laughter.	Interprets	False	mouvement	Inferred relationship	Some	7
Autosomal recessive spastic paraplegia type 27 is a rare, pure or complex hereditary spastic paraplegia characterized by a variable onset of slowly progressive lower limb spasticity, hyperreflexia and extensor plantar responses, that may be associated with sensorimotor polyneuropathy, decreased vibration sense, lower limb distal muscle wasting, dysarthria and mild to moderate intellectual disability.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare complex hereditary spastic paraplegia characterized by adulthood-onset of slowly progressive, bilateral, mainly lower limb spasticity and distal weakness associated with lower limb pain, hyperreflexia, and reduced vibration sense. Axonal neuropathy is frequently observed on electromyography and nerve conduction examination.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare, pure or complex form of hereditary spastic paraplegia, with variable phenotype, typically characterized by childhood-onset of minimally progressive, bilateral, mainly symmetric lower limb spasticity and weakness, associated with pes cavus, scoliosis, sphincter disturbances and/or urinary bladder hyperactivity. Rare additional associated manifestations may include mild intellectual disability, axonal motor neuropathy, and seizures.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare, genetic, syndromic intellectual disability disorder characterized by intellectual disability, significant motor delay, severe speech impairment, early-onset truncal hypotonia with progressive distal hypertonia/spasticity, microcephaly, and behavioral anomalies (autistic features, aggression or auto-aggressive behavior, sleep disturbances). Variable facial dysmorphism includes broad nasal tip with small alae nasi, long and/or flat philtrum, thin upper lip vermillion. Visual impairment (strabismus, hyperopia, myopia) is commonly associated.	Interprets	False	mouvement	Inferred relationship	Some	5
A rare, complex hereditary spastic paraplegia disorder characterized by infantile onset of progressive lower limb spasticity, global developmental delay, hyperreflexia, clonus and extensor plantar reflexes, associated with dysarthria, intellectual disability, cataracts and hearing impairment.	Interprets	False	mouvement	Inferred relationship	Some	6
A type of autosomal recessive pure hereditary spastic paraplegia characterized by infancy onset of crural spastic paraparesis with scissors gait, extensor plantar response, and increased tendon reflexes. Neuroimaging reveals a thin corpus callosum and electromyography and nerve conduction velocity studies are normal.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare autosomal dominant pure hereditary spastic paraplegia characterized by early childhood onset of slowly progressive crural spastic paraparesis presenting with spastic gait, mild stiffness at rest, hyperreflexia (in lower limbs), extensor plantar responses and, in some, mild postural tremor, pes cavus, sphincter disturbances and sensory loss at ankles.	Interprets	False	mouvement	Inferred relationship	Some	6
Autosomal recessive spastic paraplegia type 60 is a rare, complex hereditary spastic paraplegia disorder characterized by infantile onset of progressive lower limb spasticity, inability to walk, hypertonia and impaired vibration sense at ankles, with complicating signs including sensory impairment, nystagmus, motor axonal neuropathy and mild intellectual disability.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare, complex hereditary spastic paraplegia disorder characterized by infantile onset of progressive lower limb spasticity, severe gait disturbances leading to a non-ambulatory state, absent deep tendon reflexes and amyotrophy. Additional signs include severe sensorimotor neuropathy, pes equinovarus and mild intellectual disability. Cerebellar and corpus callosum hypoplasia, as well as colpocephaly, are observed on neuroimaging.	Interprets	False	mouvement	Inferred relationship	Some	6
Inherited congenital spastic tetraplegia is a rare, genetic, neurological disease characterized by non-progressive, variable spastic quadriparesis in multiple members of a family, in the absence of additional factors complicating pregnancy or birth (e.g. perinatal asphyxia, congenital infection). Additional clinical features include congenital hypotonia, intellectual disability, and developmental delay. Dysphagia, dysarthria, exotropia, nystagmus, seizures and brain atrophy with ventriculomegaly may be also present.	Interprets	False	mouvement	Inferred relationship	Some	4
Autosomal recessive spastic paraplegia type 14 is a rare, complex hereditary spastic paraplegia characterized by adulthood-onset of slowly progressive spastic paraplegia of lower limbs presenting with spastic gait, hyperreflexia, and mild lower limb hypertonicity associated with mild intellectual disability, visual agnosia, short and long-term memory deficiency and mild distal motor neuropathy. Bilateral pes cavus and extensor plantar responses are also associated.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare genetic peripheral neuropathy characterized by early hypotonia evolving to spastic paraparesis, areflexia, decreased pain and temperature sensitivity, autonomic neuropathy, gastroesophageal reflux disease, recurrent pneumonia and respiratory problems. Patients also have intellectual disability and dysmorphic features, including mild brachycephalic microcephaly, short broad neck, low anterior hairline and coarse face.	Interprets	False	mouvement	Inferred relationship	Some	9
A complex hereditary spastic paraplegia characterised by mild to severe lower limb spasticity, hyperreflexia, extensor plantar responses, impaired vibration sensation, pes cavus, and significant wasting and weakness of the small hand muscles. Temporal lobe epilepsy and cognitive dysfunction have been also reported.	Interprets	False	mouvement	Inferred relationship	Some	6
A complex, hereditary, spastic paraplegia characterized by delayed motor development, spasticity, and inability to walk, later progressing to quadriplegia, motor aphasia, bowel and bladder dysfunction. Patients also present with vision problems and mild intellectual disability. The disease affects only males.	Interprets	False	mouvement	Inferred relationship	Some	2
A rare, pure or complex form of hereditary spastic paraplegia characterized by progressive spastic paraplegia with pyramidal signs in the upper and lower limbs, and decreased vibration sense.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare form of hereditary spastic paraplegia characterized by delayed walking, toe walking, unsteady and spastic gait, hyperreflexia of the lower limbs, and extensor plantar responses. Upper limbs spasticity and dystonia, subclinical axonal neuropathy, cognitive impairment and intellectual disability have also been associated.	Interprets	False	mouvement	Inferred relationship	Some	6
A very rare, pure form of spastic paraplegia characterized by an onset in infancy of lower limb spasticity associated with gait disturbances, scissor gait, tiptoe walking, clonus and increased deep tendon reflexes. Mild upper limb involvement may occasionally also be associated.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare, pure or complex form of hereditary spastic paraplegia characterized by early adulthood onset of slowly progressive lower limb spasticity resulting in gait disturbances, hyperreflexia and extensor plantar responses, urinary urgency and/or incontinence, muscle weakness, decreased vibration sense and mild muscular atrophy in lower extremities. It may be associated with complicating signs, such as sensory neuropathy, ataxia (i.e. mild dysmetria, uncoordinated eye movement) and mild dysphagia.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare, genetic, non-dystrophic myopathy disease characterized by childhood-onset severe external ophthalmoplegia, typically without ptosis, associated with mild, very slowly progressive muscular weakness and atrophy, involving the facial, neck flexor and limb (upper > lower, proximal > distal) muscles. Muscle biopsy shows type 1 fiber uniformity, absent, or abnormally small, type 2A fibers, increased variability of fiber size, internalized nuclei and/or fatty infiltration.	Interprets	False	mouvement	Inferred relationship	Some	7
Bilateral progressive external ophthalmoplegia	Interprets	False	mouvement	Inferred relationship	Some	6
Hemiparesis of left side of face (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Hemiparesis of right side of face (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Autosomal dominant progressive external ophthalmoplegia type 5	Interprets	False	mouvement	Inferred relationship	Some	5
Autosomal dominant progressive external ophthalmoplegia type 3 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Autosomal dominant progressive external ophthalmoplegia type 4 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Autosomal dominant progressive external ophthalmoplegia type 1 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Atypical progressive supranuclear palsy syndrome	Interprets	False	mouvement	Inferred relationship	Some	5
X-linked complex hereditary spastic paraplegia	Interprets	False	mouvement	Inferred relationship	Some	6
X-linked pure hereditary spastic paraplegia	Interprets	False	mouvement	Inferred relationship	Some	6
Progressive supranuclear palsy corticobasal syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Progressive supranuclear palsy progressive non fluent aphasia	Interprets	False	mouvement	Inferred relationship	Some	5
Exophthalmic ophthalmoplegia	Interprets	False	mouvement	Inferred relationship	Some	4
Monoparesis of lower limb	Interprets	False	mouvement	Inferred relationship	Some	4
Hemiplegia and/or hemiparesis following stroke	Interprets	False	mouvement	Inferred relationship	Some	3
Ophthalmoplegia due to diabetes mellitus (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Hemiparesis as late effect of cerebrovascular disease	Interprets	False	mouvement	Inferred relationship	Some	5
Monoplegia of arm dominant side as sequela of cerebrovascular disease	Interprets	False	mouvement	Inferred relationship	Some	6
A rare complex hereditary spastic paraplegia characterized by neonatal to infantile onset of progressive spasticity in the lower limbs, hyperreflexia, tip-toe walking, pes equinus, and delayed motor developmental milestones. Kyphoscoliosis becomes evident in older patients, and most patients show atrophy of the lateral aspects of the tongue. Additional signs may include intellectual disability, language impairment, and moderate upper limb involvement.	Interprets	False	mouvement	Inferred relationship	Some	7
Autosomal recessive spastic paraplegia type 76 is a rare, complex hereditary spastic paraplegia characterized by adult onset slowly progressive, mild to moderate lower limb spasticity and hyperreflexia, resulting in gait disturbances, commonly associated with upper limb hyperreflexia and dysarthria. Foot deformities (usually pes cavus) and extensor plantar responses are also frequent. Additional features may include ataxia, lower limb weakness/amyotrophy, abnormal bladder function, distal sensory loss and mild intellectual deterioration.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare genetic neurological disorder characterized by postnatal microcephaly, hypotonia during infancy followed in most cases by progressive spasticity mainly affecting the lower limbs, and spastic diplegia or paraplegia, intellectual disability, delayed or absent speech, and dysarthria. Seizures and mildly dysmorphic features have been described in some patients.	Interprets	False	mouvement	Inferred relationship	Some	8
Autosomal recessive spastic paraplegia type 74 is a rare, genetic, spastic paraplegia-optic atrophy-neuropathy-related (SPOAN-like) disorder characterized by childhood onset of mild to moderate spastic paraparesis which manifests with gait impairment that very slowly progresses into late adulthood, hyperactive patellar reflex and bilateral extensor plantar response, in association with optic atrophy and typical symptoms of peripheral neuropathy, including reduced or absent ankle reflexes, lower limb atrophy and distal sensory impairment. Reduced visual acuity and pes cavus are frequently reported.	Interprets	False	mouvement	Inferred relationship	Some	5
Hereditary spastic paraplegia	Interprets	False	mouvement	Inferred relationship	Some	6
A rare genetic neurological disorder characterized by progressive spastic paraparesis and delayed gross motor development with an onset in infancy or early childhood. Patients also show variable degrees of intellectual disability, speech delay, and dysarthria. Other reported features include microcephaly, seizures, bifid uvula with or without cleft palate, and ocular anomalies. Brain imaging shows white matter abnormalities in the periventricular and other regions.	Interprets	False	mouvement	Inferred relationship	Some	7
Spastic paraplegia-severe developmental delay-epilepsy syndrome is a rare, genetic, complex spastic paraplegia disorder characterized by an infantile-onset of psychomotor developmental delay with severe intellectual disability and poor speech acquisition, associated with seizures (mostly myoclonic), muscular hypotonia which may be noted at birth, and slowly progressive spasticity in the lower limbs leading to severe gait disturbances. Ocular abnormalities and incontinence are commonly associated. Other symptoms may include verbal dyspraxia, hypogenitalism, macrocephaly and sensorineural hearing loss, as well as dystonic movements and ataxia with upper limb involvement.	Interprets	False	mouvement	Inferred relationship	Some	8
Autosomal dominant hereditary spastic paraplegia	Interprets	False	mouvement	Inferred relationship	Some	4
X-linked hereditary spastic paraplegia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Autosomal recessive hereditary spastic paraplegia	Interprets	False	mouvement	Inferred relationship	Some	4
A rare predominantly pure hereditary spastic paraplegia characterized by juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances, and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment, and urinary symptoms. Cognition is normal.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare complex hereditary spastic paraplegia characterized by juvenile to adult onset of slowly progressive spasticity mainly affecting the lower limbs, associated with spastic dysarthria and motor neuropathy. Additional manifestations include congenital bilateral cataract, gastroesophageal reflux, persistent vomiting, mild cerebellar signs, pes cavus, and occasionally short stature, among others.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare complex hereditary spastic paraplegia characterized by early onset of slowly progressive spastic para- or tetraparesis, increased tendon reflexes, positive Babinski sign, global developmental delay, cognitive impairment, and pseudobulbar palsy. Additional manifestations include dysmorphic facial features, tremor, short stature, and urinary incontinence.	Interprets	False	mouvement	Inferred relationship	Some	6
A pure form of hereditary spastic paraplegia characterized by adult onset of crural spastic paraparesis, hyperreflexia, extensor plantar responses, proximal muscle weakness, mild muscle atrophy, decreased vibration sensation at ankles, and mild urinary dysfunction. Foot deformities have been reported to eventually occur in some patients. No abnormalities are noted on brain magnetic resonance imaging and peripheral nerve conduction velocity studies.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare, complex hereditary spastic paraplegia characterized by an early onset and slow progression of spastic paraplegia associated with cerebellar signs, nystagmus, peripheral neuropathy, extensor plantar responses and borderline to mild intellectual disability. Additional features of hypo- or areflexia, mild upper limb involvement and significant visual impairment (optic atrophy, vision loss, astigmatism) have been reported.	Interprets	False	mouvement	Inferred relationship	Some	6
Autosomal recessive spastic paraplegia type 77 is a rare, pure or complex hereditary spastic paraplegia characterized by an infancy to childhood onset of slowly progressive lower limb spasticity, delayed motor milestones, gait disturbances, hyperreflexia and various muscle abnormalities, including weakness, hypotonia, intention tremor and amyotrophy. Ocular abnormalities (e.g. strabismus, ptosis) and other neurological abnormalities, such as dysarthria, seizures and extensor plantar responses, may also be associated.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare autosomal recessive complex spastic paraplegia characterized by mostly adult-onset progressive spasticity and weakness predominantly affecting the lower limbs, axonal motor and sensory neuropathy, and cerebellar symptoms like ataxia, dysarthria, and oculomotor abnormalities. Variable degrees of cognitive impairment may also be present. Subtle extrapyramidal involvement and supranuclear gaze palsy were reported in some cases. Features on brain imaging include cerebral and cerebellar atrophy and sometimes abnormalities of the corpus callosum or basal ganglia.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare genetic neurological disorder characterized by neonatal onset of rigidity and intractable seizures, with episodic jerking already beginning in utero. Affected infants have small heads, remain visually inattentive, do not feed independently, and make no developmental progress. Frequent spontaneous apnea and bradycardia usually culminate in cardiopulmonary arrest and death in infancy, although some cases were described with a milder clinical course and survival into childhood.	Interprets	False	mouvement	Inferred relationship	Some	5
Acquired horizontal gaze palsy (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Ophthalmoplegia due to abetalipoproteinemia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Isolated acquired horizontal gaze palsy (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
A rare syndromic disorder with strabismus with characteristics of congenital non-progressive ophthalmoplegia affecting the oculomotor and/or trochlear nucleus/nerve and their innervated muscles. Patients present with abnormal resting position of the eyes (in most cases infraducted and exotropic), limitation of vertical and horizontal gaze, impaired binocular vision, amblyopia, unilateral or bilateral blepharoptosis, and compensatory abnormal head posture. Extraocular manifestations include intellectual disability, peripheral neuropathy, and skeletal abnormalities among others.	Interprets	False	mouvement	Inferred relationship	Some	5
Congenital horizontal gaze palsy (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Isolated congenital horizontal gaze paresis	Interprets	False	mouvement	Inferred relationship	Some	3
Intermittent horizontal conjugate gaze deviation (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Intermittent upward gaze deviation (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Horizontal gaze preference (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Ophthalmoplegia due to and following Guillain-Barré syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	6
Ophthalmoplegia due to neuropathy (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Paralysis of downgaze	Interprets	False	mouvement	Inferred relationship	Some	3
Paralysis of upgaze (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Combined paralysis of upgaze and downgaze	Interprets	False	mouvement	Inferred relationship	Some	3
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	False	mouvement	Inferred relationship	Some	3
Wall-eyed bilateral internuclear ophthalmoplegia syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
A rare syndromic intellectual deficiency characterized by psychomotor delay, severe progressive spastic quadriplegia, microcephaly, and a Hallermann-Streiff-like phenotype including absence of eyebrows and eyelashes, glaucoma, and small, beaked nose. Structural central nervous system abnormalities (cervical spinal cyst, occipital cranium bifidum occulatum) were additional findings. There have been no further descriptions in the literature since 1974.	Interprets	False	mouvement	Inferred relationship	Some	10
A rare, genetic, syndromic intellectual disability disorder characterized by congenital, external, nuclear ophthalmoplegia, lingua scrotalis, progressive chorioretinal sclerosis and intellectual disability. Bilateral ptosis, bilateral facial weakness, Parinaud's syndrome, convergence paresis and myopia may be associated. There have been no further descriptions in the literature since 1975.	Interprets	False	mouvement	Inferred relationship	Some	8
A rare autosomal ichthyosis syndrome with prominent neurologic signs characterized by the association of congenital ichthyosis with global developmental delay, intellectual disability, infantile-onset seizures, and spastic tetraplegia. Brain imaging may show delayed myelination and cerebral atrophy. Marked intrafamilial variability has been reported.	Interprets	False	mouvement	Inferred relationship	Some	8
Vertical one-and-a-half syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
A rare, genetic, syndromic intellectual disability disorder characterized by the association of nonprogressive spastic quadriparesis, retinitis pigmentosa, intellectual disability, and variable deafness. There have been no further descriptions in the literature since 1976.	Interprets	False	mouvement	Inferred relationship	Some	7
A rare leukodystrophy characterized by a spectrum of progressive neurologic manifestations comprising rapidly progressive early-onset nystagmus, spastic tetraplegia, and visual and hearing impairment, resulting in death in early childhood, as well as later onset of slowly progressive complex spastic ataxia with pyramidal and cerebellar symptoms and loss of developmental milestones. Brain imaging shows diffuse hypomyelination of the subcortical and deep white matter, cerebellar atrophy, and diffuse spinal cord volume loss.	Interprets	False	mouvement	Inferred relationship	Some	12
Periodic alternating gaze deviation	Interprets	False	mouvement	Inferred relationship	Some	3
Ophthalmoplegia due to phytanic acid storage disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Sustained upward gaze deviation (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Sustained horizontal conjugate gaze deviation, contralateral type (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Sustained horizontal conjugate gaze deviation, ipsilateral type (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Sustained horizontal conjugate gaze deviation	Interprets	False	mouvement	Inferred relationship	Some	4
Paralytic shellfish poisoning	Interprets	False	mouvement	Inferred relationship	Some	4
Aspergillus clavatus tremors	Interprets	False	mouvement	Inferred relationship	Some	3
Tremor due to substance withdrawal (finding)	Interprets	False	mouvement	Inferred relationship	Some	2
Impairment of motor nerve function as a complication of cutaneous surgery	Interprets	False	mouvement	Inferred relationship	Some	3
Bobble-head doll syndrome	Interprets	False	mouvement	Inferred relationship	Some	1
Amyotrophic lateral sclerosis with parkinsonism	Interprets	False	mouvement	Inferred relationship	Some	3

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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
42051000077112	mouvement	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module