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
Psychogenic tremor (disorder)	Interprets	True	Movement	Inferred relationship	Some	1
Hyperactive tongue	Interprets	True	Movement	Inferred relationship	Some	2
Peripheral facial palsy	Interprets	True	Movement	Inferred relationship	Some	3
Acute flaccid paralysis (finding)	Interprets	True	Movement	Inferred relationship	Some	3
Focal motor weakness	Interprets	True	Movement	Inferred relationship	Some	1
Mild dysfunction of the facial nerve evidenced by slight facial weakness, possible mild synkinesis, normal symmetry and tone at rest, moderate to good forehead movement, complete eye closure and slight asymmetry of the mouth.	Interprets	True	Movement	Inferred relationship	Some	4
Moderate dysfunction of the facial nerve evidenced by asymmetry of the face without disfigurement, moderate synkinesis, contracture, or hemifacial spasm, normal symmetry and tone at rest, slight to moderate movement of forehead, complete eye closure with effort and slight weakness of the mouth which persists even with maximum effort.	Interprets	True	Movement	Inferred relationship	Some	4
Moderately severe dysfunction of the facial nerve evidenced by weakness and/or asymmetry of the face causing disfigurement, normal symmetry and tone at rest, absence of forehead movement, incomplete eye closure and asymmetry of the mouth even with maximum effort.	Interprets	True	Movement	Inferred relationship	Some	4
Severe dysfunction of the facial nerve evidenced by barely perceptible movement, facial asymmetry at rest, absence of forehead movement, incomplete eye closure, and only slight movement of the mouth.	Interprets	True	Movement	Inferred relationship	Some	4
A form of dyskinetic cerebral palsy with involuntary movements accompanied by an abnormal, sustained posture.	Interprets	True	Movement	Inferred relationship	Some	4
Choreic cerebral palsy	Interprets	True	Movement	Inferred relationship	Some	4
A form of dyskinetic cerebral palsy with a combination of chorea and athetosis; movements are irregular, but twisting and curving.	Interprets	True	Movement	Inferred relationship	Some	4
Mandible deviates left on opening (finding)	Interprets	True	Movement	Inferred relationship	Some	3
Mandible deviates right on opening (finding)	Interprets	True	Movement	Inferred relationship	Some	3
Reversed peristalsis	Interprets	True	Movement	Inferred relationship	Some	4
Coarse tremor	Interprets	True	Movement	Inferred relationship	Some	1
Motor level spinal weakness	Interprets	True	Movement	Inferred relationship	Some	2
Spastic paralysis	Interprets	True	Movement	Inferred relationship	Some	4
Emprosthotonus	Interprets	True	Movement	Inferred relationship	Some	2
Metallic tremor	Interprets	True	Movement	Inferred relationship	Some	1
Decreased peristalsis	Interprets	True	Movement	Inferred relationship	Some	4
Congenital hereditary facial paralysis-variable hearing loss syndrome is an extremely rare autosomal recessive disorder characterized by bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears), and strabismus.	Interprets	True	Movement	Inferred relationship	Some	7
Acquired vocal cord paralysis in newborn (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Chorea due to heredodegenerative disorder	Interprets	True	Movement	Inferred relationship	Some	3
Tremor due to metabolic disorder	Interprets	False	Movement	Inferred relationship	Some	3
Tremor due to substance abuse	Interprets	False	Movement	Inferred relationship	Some	3
Tremor due to drug withdrawal	Interprets	False	Movement	Inferred relationship	Some	2
A rare syndromic neurological disorder characterized by the association of Möbius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. There have been no further reports since 1996.	Interprets	True	Movement	Inferred relationship	Some	3
A rare X-linked syndromic intellectual disability characterized by congenital and permanent vocal cord paralysis causing severe congenital laryngeal stridor, associated with intellectual disability in male patients. Other presenting symptoms may include weak cry, cough, cyanosis, neonatal asphyxia, feeding difficulty, aspiration, and bronchiectasis. Microcephaly, tone abnormalities, visual and hearing impairment may also be associated features.	Interprets	True	Movement	Inferred relationship	Some	3
Hereditary hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses.	Interprets	False	Movement	Inferred relationship	Some	5
Infection causing chorea (disorder)	Interprets	False	Movement	Inferred relationship	Some	2
Chorea due to and following infective disorder (disorder)	Interprets	False	Movement	Inferred relationship	Some	4
Chorea co-occurrent and due to dentatorubropallidoluysian degeneration (disorder)	Interprets	False	Movement	Inferred relationship	Some	3
Chorea co-occurrent and due to Wilson disease (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Chorea co-occurrent and due to systemic lupus erythematosus	Interprets	False	Movement	Inferred relationship	Some	3
Enhanced physiological tremor (finding)	Interprets	True	Movement	Inferred relationship	Some	1
Tremor due to central nervous system disease (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Focal myoclonus (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Functional chorea	Interprets	False	Movement	Inferred relationship	Some	2
Isolated hereditary congenital facial paralysis (IHCFP) is an extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve and has been reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal.	Interprets	True	Movement	Inferred relationship	Some	3
A rare tremor disorder characterized by an isolated high frequency (>12Hz) tremor that occurs when standing, typically in weight-bearing muscles, causing a feeling of unsteadiness or discomfort, which disappears when not standing.	Interprets	False	Movement	Inferred relationship	Some	2
Deafness-ear malformation-facial palsy syndrome is characterized by profound conductive deafness due to stapedial abnormalities associated with variable malformations of the external ears and facial paralysis. It has been described in three siblings and their mother. Inheritance is autosomal dominant.	Interprets	True	Movement	Inferred relationship	Some	5
The occurrence of abnormal involuntary movements that are incongruent with a known neurologic cause and are significantly improved on neurological exam with distraction or non-physiologic maneuvers. The disorder is defined by its clinical appearance, rather than by any causative speculation.	Interprets	True	Movement	Inferred relationship	Some	3
Flaccid monoplegia of upper limb (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Flaccid monoplegia of lower limb (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Tracheal dyskinesia (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Normal movement of uvula (finding)	Interprets	True	Movement	Inferred relationship	Some	2
An extremely rare multiple congenital anomalies/dysmorphic syndrome with characteristics of craniofacial dysmorphism including microbrachycephaly, sloping forehead, micro/anophthalmia, large ears, prominent nasal root, mild micrognathia and cleft palate. The syndrome is associated with cerebral palsy with choreoathetoid movements, intellectual disability, dextrocardia and longitudinal folding of plantae pedis. There have been no further descriptions in the literature since 1992.	Interprets	True	Movement	Inferred relationship	Some	6
A rare peripheral neuropathy with characteristics of 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	Inferred relationship	Some	3
A rare neurologic disease with characteristics of excessive startle response to unexpected auditory, tactile or visual stimuli, associated with hyperreflexia.	Interprets	False	Movement	Inferred relationship	Some	5
A form of dyskinetic cerebral palsy with slow, writhing movements that are often repetitive, sinuous, and rhythmic.	Interprets	True	Movement	Inferred relationship	Some	4
Tick paralysis	Interprets	True	Movement	Inferred relationship	Some	3
A rare slowly progressive genetic peripheral neuropathy with characteristics of distal atrophy and weakness affecting the upper limbs (with a predilection for the thenar eminence) and subsequently the lower limbs, associated with unilateral or bilateral vocal cord paresis leading to hoarse voice, breathing difficulties and facial weakness.	Interprets	True	Movement	Inferred relationship	Some	5
A rare hereditary disorder with 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	Inferred relationship	Some	6
Familial dyskinesia and facial myokymia is a rare paroxysmal movement disorder, with childhood or adolescent onset, characterized by paroxysmal choreiform, dystonic, and myoclonic movements involving the limbs (mostly distal upper limbs), neck and/or face, which can progressively increase in both frequency and severity until they become nearly constant. Patients may also present with delayed motor milestones, perioral and periorbital dyskinesias, dysarthria, hypotonia, and weakness.	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis of left vocal cord (disorder)	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis of right vocal cord	Interprets	True	Movement	Inferred relationship	Some	3
Normal upper limb movement and sensation and circulation (finding)	Interprets	True	Movement	Inferred relationship	Some	3
Normal lower limb movement and sensation and circulation (finding)	Interprets	True	Movement	Inferred relationship	Some	3
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	Inferred relationship	Some	4
A rare genetic neuromuscular disease characterised by normokalaemic episodes of painful muscle cramping followed by progressive permanent flaccid weakness. Triggered by stress, cold and exercise and associated with myopathic myopathy and painful acute oedema with neuronal compression, foot drop and muscle degeneration when located in the tibialis anterior muscle group.	Interprets	True	Movement	Inferred relationship	Some	4
A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.	Interprets	True	Movement	Inferred relationship	Some	4
Flail elbow	Interprets	True	Movement	Inferred relationship	Some	2
Trismus	Interprets	True	Movement	Inferred relationship	Some	1
Hyperextension	Interprets	True	Movement	Inferred relationship	Some	2
Laryngeal hemiplegia	Interprets	True	Movement	Inferred relationship	Some	4
Neonatal dyskinesia	Interprets	True	Movement	Inferred relationship	Some	3
Ulnar neuropraxia	Interprets	True	Movement	Inferred relationship	Some	3
Post-hemiplegic tremor	Interprets	True	Movement	Inferred relationship	Some	1
Tongue deviation disorder of twelfth cranial nerve	Interprets	True	Movement	Inferred relationship	Some	3
Dyskinesia	Interprets	True	Movement	Inferred relationship	Some	2
Flail motion	Interprets	True	Movement	Inferred relationship	Some	1
Pharyngeal paralysis	Interprets	True	Movement	Inferred relationship	Some	3
Paralysis of larynx	Interprets	True	Movement	Inferred relationship	Some	3
Tremor due to orthostatic hypotension (finding)	Interprets	True	Movement	Inferred relationship	Some	2
A rare X-linked syndromic intellectual disability disease with characteristics of neonatal hypertonia which evolves to hypotonia and an exaggerated startle response (to sudden visual, auditory or tactile stimuli), followed by the development of early-onset, frequently refractory, tonic or myoclonic seizures. Progressive epileptic encephalopathy, intellectual disability, and psychomotor development arrest, with subsequent decline, may be additionally associated. There is the disease is caused by mutation in the ARHGEF9 gene on chromosome Xq22.1.	Interprets	True	Movement	Inferred relationship	Some	6
Contracture of muscle following injury	Interprets	True	Movement	Inferred relationship	Some	3
Complete paralysis of left vocal cord	Interprets	True	Movement	Inferred relationship	Some	3
Complete paralysis of right vocal cord	Interprets	True	Movement	Inferred relationship	Some	3
Total paralysis of the facial nerve.	Interprets	True	Movement	Inferred relationship	Some	4
Dissociative neurological symptom disorder co-occurrent with chorea	Interprets	False	Movement	Inferred relationship	Some	1
Dissociative neurological symptom disorder co-occurrent with myoclonus (disorder)	Interprets	True	Movement	Inferred relationship	Some	2
Dissociative neurological symptom disorder co-occurrent with tremor	Interprets	False	Movement	Inferred relationship	Some	1
Propriospinal myoclonus at sleep onset	Interprets	True	Movement	Inferred relationship	Some	2
Normal abdominal wall movement (finding)	Interprets	True	Movement	Inferred relationship	Some	3
Muscle paralysis due to and following neuromuscular blockade (disorder)	Interprets	True	Movement	Inferred relationship	Some	5
Tremor in bilateral outstretched hands (finding)	Interprets	True	Movement	Inferred relationship	Some	4
Tremor of tongue	Interprets	True	Movement	Inferred relationship	Some	2
Huntington's chorea	Interprets	False	Movement	Inferred relationship	Some	2
Juvenile onset Huntington's disease	Interprets	False	Movement	Inferred relationship	Some	1
Late onset Huntington's disease	Interprets	False	Movement	Inferred relationship	Some	1
Akinetic-rigid form of Huntington's disease	Interprets	False	Movement	Inferred relationship	Some	1
Synkinesis of left lower eyelid (finding)	Interprets	False	Movement	Inferred relationship	Some	3
Synkinesis of right lower eyelid	Interprets	False	Movement	Inferred relationship	Some	3
Crutch paralysis (disorder)	Interprets	True	Movement	Inferred relationship	Some	4
Finding of movement of sacrum (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Posterior movement of the base of the sacrum in relation to the ilia.	Interprets	True	Movement	Inferred relationship	Some	2
Sacral flexion (finding)	Interprets	True	Movement	Inferred relationship	Some	1
Anterior sacral nutation (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Sacral nutation (finding)	Interprets	True	Movement	Inferred relationship	Some	2
Extension of right side of sacral spine	Interprets	True	Movement	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
2235911000005118	Bevægelse	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)