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255324009: Movement (observable entity)

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

327 descendants. Search Descendants:

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
Monoplegia of upper limb due to and following ischemic cerebrovascular accident (disorder) Interprets True Movement Inferred relationship Some 6
Hemiplegia of nondominant side due to and following embolic cerebrovascular accident (disorder) Interprets True Movement Inferred relationship Some 5
Paraplegia due to and following cerebrovascular accident (disorder) Interprets True Movement Inferred relationship Some 6
Acute paralytic poliomyelitis, vaccine-associated Interprets True Movement Inferred relationship Some 5
Acute bulbar poliomyelitis caused by Human poliovirus 2 Interprets True Movement Inferred relationship Some 4
Acute bulbar poliomyelitis caused by Human poliovirus 1 Interprets True Movement Inferred relationship Some 4
Acute paralytic poliomyelitis caused by Human poliovirus 1 (disorder) Interprets True Movement Inferred relationship Some 4
Acute paralytic poliomyelitis caused by Human poliovirus 2 Interprets True Movement Inferred relationship Some 4
Acute paralytic poliomyelitis caused by Human poliovirus 3 (disorder) Interprets True Movement Inferred relationship Some 4
Congenital fibrosis of inferior rectus muscle (disorder) Interprets True Movement Inferred relationship Some 5
Severe intellectual disability and progressive spastic paraplegia Interprets True Movement Inferred relationship Some 7
Autosomal recessive spastic paraplegia type 27 Interprets True Movement Inferred relationship Some 6
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) Interprets True Movement Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 3 (disorder) Interprets True Movement Inferred relationship Some 6
Severe intellectual disability, progressive spastic diplegia syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 69 Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 71 Interprets True Movement Inferred relationship Some 6
Autosomal spastic paraplegia type 72 Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 60 Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 66 Interprets True Movement Inferred relationship Some 6
Inherited congenital spastic tetraplegia Interprets True Movement Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 14 Interprets True Movement Inferred relationship Some 6
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Interprets True Movement Inferred relationship Some 9
Autosomal dominant spastic paraplegia type 38 (disorder) Interprets True Movement Inferred relationship Some 6
X-linked spastic paraplegia type 16 (disorder) Interprets True Movement Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 13 (disorder) Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 56 (disorder) Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 24 Interprets True Movement Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 8 Interprets True Movement Inferred relationship Some 6
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder) Interprets True Movement Inferred relationship Some 7
Bilateral progressive external ophthalmoplegia Interprets True Movement Inferred relationship Some 6
Hemiparesis of left side of face (disorder) Interprets True Movement Inferred relationship Some 3
Hemiparesis of right side of face (disorder) Interprets True Movement Inferred relationship Some 3
Autosomal dominant progressive external ophthalmoplegia type 5 Interprets True Movement Inferred relationship Some 5
Autosomal dominant progressive external ophthalmoplegia type 3 (disorder) Interprets True Movement Inferred relationship Some 5
Autosomal dominant progressive external ophthalmoplegia type 4 (disorder) Interprets True Movement Inferred relationship Some 5
Autosomal dominant progressive external ophthalmoplegia type 1 (disorder) Interprets True Movement Inferred relationship Some 5
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Interprets True Movement Inferred relationship Some 5
Atypical progressive supranuclear palsy syndrome Interprets True Movement Inferred relationship Some 5
X-linked complex hereditary spastic paraplegia Interprets True Movement Inferred relationship Some 6
X-linked pure hereditary spastic paraplegia Interprets True Movement Inferred relationship Some 6
Progressive supranuclear palsy corticobasal syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Progressive supranuclear palsy progressive non fluent aphasia Interprets True Movement Inferred relationship Some 5
Exophthalmic ophthalmoplegia Interprets True Movement Inferred relationship Some 4
Monoparesis of lower limb Interprets True Movement Inferred relationship Some 4
Hemiplegia and/or hemiparesis following stroke Interprets True Movement Inferred relationship Some 3
Ophthalmoplegia due to diabetes mellitus (disorder) Interprets True Movement Inferred relationship Some 4
Hemiparesis as late effect of cerebrovascular disease Interprets True Movement Inferred relationship Some 5
Monoplegia of arm dominant side as sequela of cerebrovascular disease Interprets True Movement Inferred relationship Some 6
Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome Interprets True Movement Inferred relationship Some 7
Autosomal recessive spastic paraplegia type 76 (disorder) Interprets True Movement Inferred relationship Some 6
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Interprets True Movement Inferred relationship Some 8
Autosomal recessive spastic paraplegia type 74 Interprets True Movement Inferred relationship Some 5
Hereditary spastic paraplegia Interprets True Movement Inferred relationship Some 6
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) Interprets True Movement Inferred relationship Some 7
Spastic paraplegia, severe developmental delay, epilepsy syndrome Interprets True Movement Inferred relationship Some 8
Autosomal dominant hereditary spastic paraplegia Interprets True Movement Inferred relationship Some 4
X-linked hereditary spastic paraplegia (disorder) Interprets True Movement Inferred relationship Some 4
Autosomal recessive hereditary spastic paraplegia Interprets True Movement Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 9B Interprets True Movement Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 9A Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 9B Interprets True Movement Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 73 Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 75 (disorder) Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 77 Interprets True Movement Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 78 (disorder) Interprets True Movement Inferred relationship Some 6
Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Acquired horizontal gaze palsy (disorder) Interprets True Movement Inferred relationship Some 3
Ophthalmoplegia due to abetalipoproteinemia (disorder) Interprets True Movement Inferred relationship Some 4
Isolated acquired horizontal gaze palsy (disorder) Interprets True Movement Inferred relationship Some 3
Congenital fibrosis syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Congenital horizontal gaze palsy (disorder) Interprets True Movement Inferred relationship Some 4
Isolated congenital horizontal gaze paresis Interprets True Movement Inferred relationship Some 3
Intermittent horizontal conjugate gaze deviation (disorder) Interprets True Movement Inferred relationship Some 5
Intermittent upward gaze deviation (disorder) Interprets True Movement Inferred relationship Some 5
Horizontal gaze preference (disorder) Interprets True Movement Inferred relationship Some 4
Ophthalmoplegia due to and following Guillain-Barré syndrome (disorder) Interprets True Movement Inferred relationship Some 6
Ophthalmoplegia due to neuropathy (disorder) Interprets True Movement Inferred relationship Some 5
Paralysis of downgaze Interprets True Movement Inferred relationship Some 3
Paralysis of upgaze (disorder) Interprets True Movement Inferred relationship Some 3
Combined paralysis of upgaze and downgaze Interprets True Movement Inferred relationship Some 3
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder) Interprets True Movement Inferred relationship Some 3
Wall-eyed bilateral internuclear ophthalmoplegia syndrome (disorder) Interprets True Movement Inferred relationship Some 5
Pseudoprogeria syndrome (disorder) Interprets True Movement Inferred relationship Some 10
Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (disorder) Interprets True Movement Inferred relationship Some 8
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder) Interprets True Movement Inferred relationship Some 8
Vertical one-and-a-half syndrome (disorder) Interprets True Movement Inferred relationship Some 3
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (disorder) Interprets True Movement Inferred relationship Some 7
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) Interprets True Movement Inferred relationship Some 12
Periodic alternating gaze deviation Interprets True Movement Inferred relationship Some 3
Ophthalmoplegia due to phytanic acid storage disease (disorder) Interprets True Movement Inferred relationship Some 5
Sustained upward gaze deviation (disorder) Interprets True Movement Inferred relationship Some 3
Sustained horizontal conjugate gaze deviation, contralateral type (disorder) Interprets True Movement Inferred relationship Some 4
Sustained horizontal conjugate gaze deviation, ipsilateral type (disorder) Interprets True Movement Inferred relationship Some 4
Sustained horizontal conjugate gaze deviation Interprets True Movement Inferred relationship Some 4
Paralytic shellfish poisoning Interprets True Movement Inferred relationship Some 4
Aspergillus clavatus tremors Interprets True Movement Inferred relationship Some 3
Tremor due to substance withdrawal (finding) Interprets True Movement Inferred relationship Some 2
Impairment of motor nerve function as a complication of cutaneous surgery Interprets True Movement Inferred relationship Some 3
Bobble-head doll syndrome Interprets True Movement Inferred relationship Some 1
Amyotrophic lateral sclerosis with parkinsonism Interprets True Movement Inferred relationship Some 3

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