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
A type of cerebral palsy defined by increased tone and pathological reflexes resulting in an abnormal pattern of movement and posture.	Interprets	False	mouvement	Inferred relationship	Some	4
Vertical retraction syndrome	Interprets	False	mouvement	Inferred relationship	Some	5
Horizontal gaze palsy	Interprets	False	mouvement	Inferred relationship	Some	3
Congenital quadriplegia	Interprets	False	mouvement	Inferred relationship	Some	4
Millard-Gubler syndrome	Interprets	False	mouvement	Inferred relationship	Some	6
Right hemiplegia	Interprets	False	mouvement	Inferred relationship	Some	3
Left hemiplegia	Interprets	False	mouvement	Inferred relationship	Some	3
Right hemiparesis	Interprets	False	mouvement	Inferred relationship	Some	4
Left hemiparesis	Interprets	False	mouvement	Inferred relationship	Some	4
Monoparesis - arm (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Vertical gaze palsy	Interprets	False	mouvement	Inferred relationship	Some	3
Horizontal spasm of gaze	Interprets	False	mouvement	Inferred relationship	Some	3
Cerebral palsy, not congenital or infantile, acute	Interprets	False	mouvement	Inferred relationship	Some	4
Residual hemiplegia	Interprets	False	mouvement	Inferred relationship	Some	4
Spastic diplegia	Interprets	False	mouvement	Inferred relationship	Some	3
Paralysis from birth trauma (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Congenital paraplegia	Interprets	False	mouvement	Inferred relationship	Some	6
Pontine one and a half syndrome	Interprets	False	mouvement	Inferred relationship	Some	4
Alternating hemiplegia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Paralytic syndrome as late effect of stroke (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Monoplegia of lower limb affecting dominant side (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Monoplegia of upper limb affecting non-dominant side (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Monoplegia of lower limb affecting non-dominant side (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Supranuclear gaze palsy (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Paralytic syndrome as late effect of thalamic stroke (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Monoplegia of dominant lower limb as a late effect of cerebrovascular accident (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Monoplegia of dominant upper limb as a late effect of cerebrovascular accident (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Hemiplegia of nondominant side	Interprets	False	mouvement	Inferred relationship	Some	3
Spastic hemiplegia of nondominant side	Interprets	False	mouvement	Inferred relationship	Some	3
Monoplegia of lower limb as late effect of cerebrovascular disease	Interprets	False	mouvement	Inferred relationship	Some	5
Spastic hemiplegia of dominant side	Interprets	False	mouvement	Inferred relationship	Some	3
Monoplegia of nondominant lower limb as a late effect of cerebrovascular accident	Interprets	False	mouvement	Inferred relationship	Some	5
Monoplegia of upper limb of dominant side	Interprets	False	mouvement	Inferred relationship	Some	3
Hemiparesis as late effect of cerebrovascular accident	Interprets	False	mouvement	Inferred relationship	Some	5
Flaccid hemiplegia of dominant side	Interprets	False	mouvement	Inferred relationship	Some	3
Hemiplegia as late effect of cerebrovascular disease	Interprets	False	mouvement	Inferred relationship	Some	5
Flaccid hemiplegia of nondominant side	Interprets	False	mouvement	Inferred relationship	Some	3
Monoplegia of upper limb as late effect of cerebrovascular disease	Interprets	False	mouvement	Inferred relationship	Some	5
Hemiplegia of dominant side	Interprets	False	mouvement	Inferred relationship	Some	3
Monoplegia of nondominant upper limb as a late effect of cerebrovascular accident	Interprets	False	mouvement	Inferred relationship	Some	5
Transient monoplegia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Hemiplegia of nondominant side as late effect of cerebrovascular disease	Interprets	False	mouvement	Inferred relationship	Some	5
Hemiplegia of dominant side as late effect of cerebrovascular disease	Interprets	False	mouvement	Inferred relationship	Some	5
Hemiplegia as late effect of cerebrovascular accident	Interprets	False	mouvement	Inferred relationship	Some	4
Bilateral total ophthalmoplegia	Interprets	False	mouvement	Inferred relationship	Some	5
Total ophthalmoplegia of right eye (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Total ophthalmoplegia of left eye (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Flaccid diplegia of lower extremities (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Cauda equina syndrome with neurogenic urinary bladder	Interprets	False	mouvement	Inferred relationship	Some	5
Ocular movement disorder characterised by an impaired conjugate lateral gaze due to damage of the medial longitudinal fasciculus. The right eye is the affected eye and the left eye is the contralateral eye.	Interprets	False	mouvement	Inferred relationship	Some	4
Ocular movement disorder characterized by an impaired conjugate lateral gaze due to damage of the medial longitudinal fasciculus. The left eye is the affected eye and the right eye is the contralateral eye.	Interprets	False	mouvement	Inferred relationship	Some	4
Ocular movement disorder characterized by an impaired conjugate lateral gaze due to damage of the medial longitudinal fasciculus. Both the left and right eyes are the affected eye.	Interprets	False	mouvement	Inferred relationship	Some	5
Paralytic syndrome of nondominant side as late effect of stroke (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Paralytic syndrome of dominant side as late effect of stroke (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Paralytic syndrome of all four limbs (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Paralytic syndrome on one side of the body	Interprets	False	mouvement	Inferred relationship	Some	3
Paralytic syndrome of one limb (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Paralytic syndrome on one side of the body as late effect of cerebrovascular accident	Interprets	False	mouvement	Inferred relationship	Some	5
Ataxic hemiparesis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Paraplegia with neurogenic urinary bladder	Interprets	False	mouvement	Inferred relationship	Some	6
Paralytic syndrome of both lower limbs as sequela of stroke (disorder)	Interprets	False	mouvement	Inferred relationship	Some	7
Paralytic syndrome of all four limbs as sequela of stroke (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Complete paraplegia	Interprets	False	mouvement	Inferred relationship	Some	4
Incomplete paraplegia	Interprets	False	mouvement	Inferred relationship	Some	4
Acute paraplegia	Interprets	False	mouvement	Inferred relationship	Some	5
Chronic paraplegia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Quadriplegia with quadriparesis	Interprets	False	mouvement	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting the arm and/or leg on one side of the body. An ipsilateral upper and/or lower extremity is affected.	Interprets	False	mouvement	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting all four limbs; the term bilateral hemiplegia may also be used when one side has a significantly different tone compared with the other.	Interprets	False	mouvement	Inferred relationship	Some	4
A form of spastic cerebral palsy affecting only one limb	Interprets	False	mouvement	Inferred relationship	Some	5
A form of spastic cerebral palsy affecting two limbs; usually the legs are affected more than the arms.	Interprets	False	mouvement	Inferred relationship	Some	4
Facial palsy as birth trauma	Interprets	False	mouvement	Inferred relationship	Some	5
Monoplegic cerebral palsy affecting upper limb	Interprets	False	mouvement	Inferred relationship	Some	5
Monoplegic cerebral palsy affecting lower limb	Interprets	False	mouvement	Inferred relationship	Some	5
A form of spastic cerebral palsy affecting the lower half of the body, including both legs.	Interprets	False	mouvement	Inferred relationship	Some	3
A form of cerebral palsy where no predominant motion can be determined; when it is a mixed CP form, i.e. spasticity with ataxia and/or dyskinesia, the child should be classified according to the dominant clinical feature	Interprets	False	mouvement	Inferred relationship	Some	4
A form of spastic cerebral palsy affecting both sides of the body; the Surveillance of Cerebral Palsy in Europe (SCPE) does not recommend the use of diplegia/quadriplegia terms, and recommends using instead the term bilateral spastic cerebral palsy and subtypes.	Interprets	False	mouvement	Inferred relationship	Some	4
A form of spastic cerebral palsy affecting three limbs; this could be both arms and a leg, or both legs and an arm. In some instances, it has referred to one upper and one lower extremity and the face.	Interprets	False	mouvement	Inferred relationship	Some	4
A form of spastic cerebral palsy affecting all four limbs with neck and head paralysis, often accompanied by eating and breathing complications.	Interprets	False	mouvement	Inferred relationship	Some	3
Allan-Herndon-Dudley syndrome	Interprets	False	mouvement	Inferred relationship	Some	9
Horizontal gaze palsy with progressive scoliosis	Interprets	False	mouvement	Inferred relationship	Some	4
Paralytic syndrome of two limbs	Interprets	False	mouvement	Inferred relationship	Some	3
Paralytic syndrome of three limbs	Interprets	False	mouvement	Inferred relationship	Some	3
Paralytic syndrome on both sides of the body (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Infantile ascending hereditary spastic paralysis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	6
Ophthalmoplegia due to Graves' disease	Interprets	False	mouvement	Inferred relationship	Some	4
Acute paralytic poliomyelitis	Interprets	False	mouvement	Inferred relationship	Some	4
A rare, complex subtype of hereditary spastic paraplegia characterized by variable onset of slowly progressive lower limb spasticity and weakness and prominent cerebellar ataxia, associated with gait disturbances, dysarthria, increased deep tendon reflexes and extensor plantar responses. Additional features may include involuntary movements (i.e. clonus, tremor, fasciculations, chorea), decreased vibration sense, oculomotor abnormalities (e.g. nystagmus) and distal amyotrophy in the upper and lower limbs.	Interprets	False	mouvement	Inferred relationship	Some	6
Autosomal recessive spastic paraplegia type 70 is a very rare, complex subtype of hereditary spastic paraplegia that presents in infancy with delayed motor development (i.e. crawling, walking) and is characterized by lower limb spasticity, increased deep tendon reflexes, extensor plantar responses, impaired vibratory sensation at ankles, amyotrophy and borderline intellectual disability. Additional signs may include gait disturbances, Achilles tendon contractures, scoliosis and cerebellar abnormalities.	Interprets	False	mouvement	Inferred relationship	Some	6
Spinal atrophy-ophthalmoplegia-pyramidal syndrome is a rare, bulbospinal muscular atrophy characterized by generalized neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness. External ophthalmoplegia and bilateral mydriasis are typical signs. There have been no further descriptions in the literature since 1994.	Interprets	False	mouvement	Inferred relationship	Some	4
Erb Duchenne palsy with neuroma due to birth trauma (disorder)	Interprets	False	mouvement	Inferred relationship	Some	8
A rare type of hereditary spastic paraplegia usually characterized by a pure phenotype of proximal weakness of the lower extremities with spastic gait and brisk reflexes, with a bimodal age of onset of either childhood or adulthood (>30 years). In some cases, it can present as a complex phenotype with additional associated manifestations including peripheral neuropathy, bulbar palsy (with dysarthria and dysphagia), distal amyotrophy, and impaired distal vibration sense.	Interprets	False	mouvement	Inferred relationship	Some	6
A pure form of hereditary spastic paraplegia characterized by onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise.	Interprets	False	mouvement	Inferred relationship	Some	6
A pure form of hereditary spastic paraplegia characterized by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood and patients presenting with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and, in rare cases, pes cavus. No abnormalities are noted on magnetic resonance imaging.	Interprets	False	mouvement	Inferred relationship	Some	6
A rare, pure or complex form of hereditary spastic paraplegia usually characterized by a pure phenotype of a slowly progressive spastic paraplegia associated with urinary incontinence with an onset in mid- to late-adulthood. A complex phenotype, with the additional findings of cognitive impairment, sensorimotor polyneuropathy, ataxia, parkinsonism, and dystonia as well as thin corpus callosum and white matter lesions (seen on brain and spine magnetic resonance imaging), has also been reported.	Interprets	False	mouvement	Inferred relationship	Some	6
A pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients.	Interprets	False	mouvement	Inferred relationship	Some	6
X-linked spastic paraplegia type 34 is a pure form of hereditary spastic paraplegia characterized by late childhood- to early adulthood-onset of slowly progressive spastic paraplegia with spastic gait and lower limb hyperreflexia, brisk tendon reflexes and ankle clonus. Lower limb pain and reduced lower limb vibratory sense is also reported in some older adult patients.	Interprets	False	mouvement	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 5A is a form of hereditary spastic paraplegia characterized by either a pure phenotype of slowly progressive spastic paraplegia of the lower extremities with bladder dysfunction and pes cavus or a complex presentation with additional manifestations including cerebellar signs, nystagmus, distal or generalized muscle atrophy and cognitive impairment. Age of onset is highly variable, ranging from early childhood to adulthood. White matter hyperintensity and cerebellar and spinal cord atrophy may be noted, on brain magnetic resonance imaging, in some patients.	Interprets	False	mouvement	Inferred relationship	Some	6
A pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.	Interprets	False	mouvement	Inferred relationship	Some	6
A pure form of hereditary spastic paraplegia characterized by a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy.	Interprets	False	mouvement	Inferred relationship	Some	6
Autosomal recessive spastic paraplegia type 28 is a pure form of hereditary spastic paraplegia characterized by a childhood or adolescent onset of slowly progressive, pure crural muscle spastic paraparesis which manifests with mild lower limb weakness, gait difficulties, extensor plantar responses, and hyperreflexia of lower extremities. Less common manifestations include cerebellar oculomotor disturbance with saccadic eye pursuit, pes cavus and scoliosis. Some patients also present pin and vibration sensory loss in distal legs.	Interprets	False	mouvement	Inferred relationship	Some	6

Start Previous Page 12 of 17 Next End

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)

Back to Start

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