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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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Movement Is a Gross motor functions (observable entity) false Inferred relationship Some
    Movement Is a Process (observable entity) false 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 False 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 False 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 False 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 False Movement Inferred relationship Some 2
    Optic ataxia Interprets False Movement Inferred relationship Some 2
    Paraneoplastic opsoclonus myoclonus syndrome Interprets False Movement Inferred relationship Some 2
    Oculomotor nerve synkinesis Interprets False 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 False Movement Inferred relationship Some 3
    Paralysis of diaphragm Interprets False Movement Inferred relationship Some 3
    Relaxation of diaphragm Interprets False Movement Inferred relationship Some 3
    Paralysis due to lesion of spinal cord (disorder) Interprets False Movement Inferred relationship Some 3
    Epidural ascending spinal paralysis Interprets False Movement Inferred relationship Some 3
    Spinal paraplegia Interprets False Movement Inferred relationship Some 4
    Acute atrophic spinal paralysis Interprets False Movement Inferred relationship Some 3
    Quadriplegic spinal paralysis (disorder) Interprets False Movement Inferred relationship Some 4
    Incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder) Interprets False Movement Inferred relationship Some 3
    Complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder) Interprets False Movement Inferred relationship Some 3
    Incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder) Interprets False Movement Inferred relationship Some 3
    Complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder) Interprets False Movement Inferred relationship Some 3
    Acute complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra Interprets False Movement Inferred relationship Some 5
    Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder) Interprets False Movement Inferred relationship Some 4
    Acute complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra Interprets False Movement Inferred relationship Some 5
    Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder) Interprets False Movement Inferred relationship Some 5
    Chronic paralysis due to lesion of spinal cord Interprets False Movement Inferred relationship Some 4
    Acute paralysis due to lesion of spinal cord (disorder) Interprets False Movement Inferred relationship Some 4
    Spastic spinal syphilitic paralysis Interprets False Movement Inferred relationship Some 4
    Paralysis of tongue Interprets False Movement Inferred relationship Some 3
    Paralysis of left side of tongue Interprets False Movement Inferred relationship Some 3
    Paralysis of right side of tongue (disorder) Interprets False Movement Inferred relationship Some 3
    Bilateral paralysis of tongue Interprets False Movement Inferred relationship Some 4
    Paralysis of palate Interprets False Movement Inferred relationship Some 3
    Paralysis of uvula Interprets False Movement Inferred relationship Some 3
    Paralysis of uvula after diphtheria (disorder) Interprets False Movement Inferred relationship Some 5
    Paralytic syndrome of bilateral lower limbs (disorder) Interprets False Movement Inferred relationship Some 4
    Tetraplegia Interprets False Movement Inferred relationship Some 3
    Painful ophthalmoplegia Interprets False Movement Inferred relationship Some 4
    Crossed hemiplegia Interprets False Movement Inferred relationship Some 3
    Ophthalmoplegia plus syndrome Interprets False Movement Inferred relationship Some 4
    Total ophthalmoplegia Interprets False 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 False Movement Inferred relationship Some 4
    Monoparesis Interprets False Movement Inferred relationship Some 3
    Spastic hemiplegia Interprets False Movement Inferred relationship Some 3
    Supranuclear paralysis Interprets False Movement Inferred relationship Some 3
    Cerebral paresis with homolateral ataxia Interprets False Movement Inferred relationship Some 3
    Alternating hypoglossal hemiplegia Interprets False Movement Inferred relationship Some 4
    Paraplegia Interprets False Movement Inferred relationship Some 4
    Acute paralytic poliomyelitis, bulbar Interprets False Movement Inferred relationship Some 4
    Monoplegia Interprets False Movement Inferred relationship Some 3
    Cerebral paraparesis Interprets False Movement Inferred relationship Some 4
    Spinal hemiplegia Interprets False Movement Inferred relationship Some 3
    Cerebral paralysis with homolateral ataxia Interprets False Movement Inferred relationship Some 3
    Monoplegia of lower limb Interprets False Movement Inferred relationship Some 3
    Flaccid hemiplegia Interprets False Movement Inferred relationship Some 3
    Klumpke-Déjerine paralysis Interprets False Movement Inferred relationship Some 3
    Transient hemiplegia Interprets False Movement Inferred relationship Some 3
    Chronic progressive paraparesis Interprets False Movement Inferred relationship Some 4
    Tolosa-Hunt syndrome is an ophthalmoplegic syndrome, affecting all age groups, characterised by 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 False Movement Inferred relationship Some 3
    Hemiplegia Interprets False Movement Inferred relationship Some 3
    Diplegia of upper limbs Interprets False Movement Inferred relationship Some 3
    Partial bilateral paralysis Interprets False Movement Inferred relationship Some 3
    Parinaud's syndrome Interprets False Movement Inferred relationship Some 4
    Locked in syndrome Interprets False Movement Inferred relationship Some 3
    Facial hemiplegia (disorder) Interprets False Movement Inferred relationship Some 3
    Cerebral hemiplegia Interprets False Movement Inferred relationship Some 3
    Monoplegia of upper limb Interprets False Movement Inferred relationship Some 3
    Spastic tetraplegia with rigidity syndrome Interprets False Movement Inferred relationship Some 4
    Progressive supranuclear ophthalmoplegia Interprets False Movement Inferred relationship Some 3
    Crossed hemiparesis Interprets False Movement Inferred relationship Some 3
    Complete bilateral paralysis Interprets False Movement Inferred relationship Some 3
    Paralytic syndrome Interprets False Movement Inferred relationship Some 2
    Triparesis Interprets False Movement Inferred relationship Some 3
    Cerebral paraplegia Interprets False Movement Inferred relationship Some 4
    Recurrent painful ophthalmoplegic neuropathy Interprets False Movement Inferred relationship Some 4
    Internuclear ophthalmoplegia Interprets False Movement Inferred relationship Some 4
    Ophthalmoplegia Interprets False Movement Inferred relationship Some 4
    Facial hemiparesis Interprets False Movement Inferred relationship Some 3
    Hemiparesis Interprets False Movement Inferred relationship Some 3
    Diplegia Interprets False Movement Inferred relationship Some 3
    Triplegia Interprets False Movement Inferred relationship Some 3
    Palsy of conjugate gaze Interprets False Movement Inferred relationship Some 4
    Infantile hemiplegia Interprets False Movement Inferred relationship Some 3
    Cerebral hemiparesis Interprets False Movement Inferred relationship Some 3
    Paraparesis Interprets False Movement Inferred relationship Some 4
    Spasm of conjugate gaze Interprets False 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 False Movement Inferred relationship Some 4
    Paralysis of vagus, spinal accessory and hypoglossal nerves Interprets False Movement Inferred relationship Some 3
    Paralytic stroke Interprets False Movement Inferred relationship Some 4
    Flaccid tetraplegia (disorder) Interprets False Movement Inferred relationship Some 3
    Spastic tetraplegia Interprets False Movement Inferred relationship Some 4
    Flaccid paraplegia Interprets False Movement Inferred relationship Some 4
    Spastic paraplegia Interprets False Movement Inferred relationship Some 4
    Acute paralytic non-bulbar poliomyelitis Interprets False Movement Inferred relationship Some 4
    Acute paralytic poliomyelitis, wild virus, imported Interprets False Movement Inferred relationship Some 4
    Acute paralytic poliomyelitis, wild virus, indigenous Interprets False Movement Inferred relationship Some 4
    Pure hereditary spastic paraplegia Interprets False Movement Inferred relationship Some 4
    Complicated hereditary spastic paraplegia Interprets False Movement Inferred relationship Some 4
    A complex hereditary spastic paraplegia characterised by progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. Association with hand muscles amyotrophy is typical. Interprets False Movement Inferred relationship Some 8
    Alternating hemiplegia of childhood Interprets False Movement Inferred relationship Some 4
    Congenital nuclear ophthalmoplegia Interprets False 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 False Movement Inferred relationship Some 4

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