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255324009: Movement (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
380509014 Movement en Synonym Active Entire term case insensitive SNOMED CT core module
380510016 Quality of movement en Synonym Active Entire term case insensitive SNOMED CT core module
2528848014 Movement (observable entity) en Fully specified name Active Entire term case insensitive SNOMED CT core module

373 descendants. Search Descendants:

Expanded Value Set

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

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