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255324009: Movement (observable entity)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1187242017 Movement, function (observable entity) en Fully specified name Inactive Initial character case insensitive SNOMED CT core
2528848014 Movement (observable entity) en Fully specified name Active Case insensitive SNOMED CT core
380509014 Movement en Synonym Active Case insensitive SNOMED CT core
380510016 Quality of movement en Synonym Active Case insensitive SNOMED CT core
646347016 Movement (qualifier value) en Fully specified name Inactive Initial character case insensitive SNOMED CT core

292 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Movement Is a Process true Inferred relationship Some
Movement Is a Gross motor functions false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Parkinsonism due to prion disease Interprets True Movement Inferred relationship Some 3
Nail dystrophy due to habit tic Interprets True Movement Inferred relationship Some 5
Callosity due to habit tic Interprets True Movement Inferred relationship Some 5
Callosity due to biting and/or chewing Interprets True Movement Inferred relationship Some 4
Drug-induced akathisia Interprets True Movement Inferred relationship Some 2
Akathisia Interprets True Movement Inferred relationship Some 2
Acute akathisia caused by drug Interprets True Movement Inferred relationship Some 4
Classical pantothenate kinase associated neurodegeneration Interprets True Movement Inferred relationship Some 2
Atypical pantothenate kinase associated neurodegeneration Interprets True Movement Inferred relationship Some 2
Toxin-induced parkinsonism Interprets True Movement Inferred relationship Some 2
Pesticide-induced Parkinsonism Interprets True Movement Inferred relationship Some 2
Dopa responsive dystonia due to sepiapterin reductase deficiency Interprets True Movement Inferred relationship Some 3
Dystonia due to Leigh syndrome Interprets True Movement Inferred relationship Some 2
Bell's palsy Interprets False Movement Inferred relationship Some 1
Paradoxical facial movements Interprets True Movement Inferred relationship Some 1
Hyperexplexia Interprets True Movement Inferred relationship Some 3
Oral dyskinesia Interprets True Movement Inferred relationship Some 2
Excessive blinking - involuntary Interprets True Movement Inferred relationship Some 3
Tremor of palate Interprets True Movement Inferred relationship Some 3
Ataxia due to mitochondrial mutations Interprets True Movement Inferred relationship Some 2
Tremor due to metabolic disorder Interprets True Movement Inferred relationship Some 2
Tremor due to substance abuse Interprets True Movement Inferred relationship Some 2
Hereditary hyperekplexia Interprets True Movement Inferred relationship Some 4
Primary progressive freezing gait Interprets True Movement Inferred relationship Some 1
Primary orthostatic tremor Interprets True Movement Inferred relationship Some 1
Chronic hiccups Interprets True Movement Inferred relationship Some 1
Tardy left ulnar nerve palsy Interprets True Movement Inferred relationship Some 1
Sporadic hyperekplexia Interprets True Movement Inferred relationship Some 4
Congenital ichthyosis, microcephalus, tetraplegia syndrome Interprets True Movement Inferred relationship Some 9
Psychogenic movement disorder Interprets True Movement Inferred relationship Some 1
Severe oculo-renal-cerebellar syndrome Interprets True Movement Inferred relationship Some 8
Familial infantile bilateral striatal necrosis Interprets True Movement Inferred relationship Some 2
Progressive myoclonic epilepsy type 7 Interprets True Movement Inferred relationship Some 3
Autoimmune generalised polymyoclonus Interprets True Movement Inferred relationship Some 2
Cerebellar ataxia with oculomotor apraxia type 4 Interprets True Movement Inferred relationship Some 5
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Interprets True Movement Inferred relationship Some 5
Primary dystonia DYT27 type Interprets True Movement Inferred relationship Some 2
Progressive myoclonic epilepsy type 9 Interprets True Movement Inferred relationship Some 3
Corticobasal syndrome Interprets True Movement Inferred relationship Some 3
Off-periods in Parkinson disease not responding to oral treatment Interprets True Movement Inferred relationship Some 2
Microphthalmia, microtia, fetal akinesia syndrome Interprets True Movement Inferred relationship Some 6
Paraneoplastic myoclonus Interprets True Movement Inferred relationship Some 2
Optic ataxia Interprets True Movement Inferred relationship Some 2
Paraneoplastic opsoclonus myoclonus syndrome Interprets True Movement Inferred relationship Some 2
Oculomotor nerve synkinesis Interprets True Movement Inferred relationship Some 3
Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome Interprets True Movement Inferred relationship Some 3
Paralysis of diaphragm Interprets True Movement Inferred relationship Some 3
Relaxation of diaphragm Interprets True Movement Inferred relationship Some 3
Paralysis due to lesion of spinal cord Interprets True Movement Inferred relationship Some 3
Epidural ascending spinal paralysis Interprets True Movement Inferred relationship Some 3
Spinal paraplegia Interprets True Movement Inferred relationship Some 4
Acute atrophic spinal paralysis Interprets True Movement Inferred relationship Some 3
Tetraplegic spinal paralysis Interprets True Movement Inferred relationship Some 4
Incomplete tetraplegia due to spinal cord lesion at C1-C4 level Interprets True Movement Inferred relationship Some 3
Complete tetraplegia due to lesion at C1-C4 level Interprets True Movement Inferred relationship Some 3
Incomplete tetraplegia due to lesion at C5-C7 level Interprets True Movement Inferred relationship Some 3
Complete tetraplegia due to lesion at C5-C7 level Interprets True Movement Inferred relationship Some 3
Acute complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra Interprets True Movement Inferred relationship Some 5
Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra Interprets True Movement Inferred relationship Some 4
Acute complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra Interprets True Movement Inferred relationship Some 5
Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra Interprets True Movement Inferred relationship Some 5
Chronic paralysis due to lesion of spinal cord Interprets True Movement Inferred relationship Some 4
Acute paralysis due to lesion of spinal cord Interprets True Movement Inferred relationship Some 4
Spastic spinal syphilitic paralysis Interprets True Movement Inferred relationship Some 4
Paralysis of tongue Interprets True Movement Inferred relationship Some 3
Paralysis of left side of tongue Interprets True Movement Inferred relationship Some 3
Paralysis of right side of tongue Interprets True Movement Inferred relationship Some 3
Bilateral paralysis of tongue Interprets True Movement Inferred relationship Some 4
Paralysis of palate Interprets True Movement Inferred relationship Some 3
Paralysis of uvula Interprets True Movement Inferred relationship Some 3
Paralysis of uvula after diphtheria Interprets True Movement Inferred relationship Some 5
Paralytic syndrome of both lower limbs Interprets True Movement Inferred relationship Some 4
Tetraplegia Interprets True Movement Inferred relationship Some 3
Painful ophthalmoplegia Interprets True Movement Inferred relationship Some 4
Crossed hemiplegia Interprets True Movement Inferred relationship Some 3
Ophthalmoplegia plus syndrome Interprets True Movement Inferred relationship Some 4
Total ophthalmoplegia Interprets True Movement Inferred relationship Some 3
Erb-Duchenne paralysis Interprets True Movement Inferred relationship Some 4
Monoparesis Interprets True Movement Inferred relationship Some 3
Spastic hemiplegia Interprets True Movement Inferred relationship Some 3
Supranuclear paralysis Interprets True Movement Inferred relationship Some 3
Cerebral paresis with homolateral ataxia Interprets True Movement Inferred relationship Some 3
Alternating hypoglossal hemiplegia Interprets True Movement Inferred relationship Some 4
Paraplegia Interprets True Movement Inferred relationship Some 4
Acute paralytic poliomyelitis, bulbar Interprets True Movement Inferred relationship Some 4
Monoplegia Interprets True Movement Inferred relationship Some 3
Cerebral paraparesis Interprets True Movement Inferred relationship Some 4
Spinal hemiplegia Interprets True Movement Inferred relationship Some 3
Cerebral paralysis with homolateral ataxia Interprets True Movement Inferred relationship Some 3
Monoplegia of lower limb Interprets True Movement Inferred relationship Some 3
Flaccid hemiplegia Interprets True Movement Inferred relationship Some 3
Klumpke-Déjerine paralysis Interprets True Movement Inferred relationship Some 3
Transient hemiplegia Interprets True Movement Inferred relationship Some 3
Chronic progressive paraparesis Interprets True Movement Inferred relationship Some 4
Tolosa-Hunt syndrome Interprets True Movement Inferred relationship Some 3
Hemiplegia Interprets True Movement Inferred relationship Some 3
Diplegia of upper limbs Interprets True Movement Inferred relationship Some 3
Partial bilateral paralysis Interprets True Movement Inferred relationship Some 3
Parinaud's syndrome Interprets True Movement Inferred relationship Some 4
Locked in syndrome Interprets True Movement Inferred relationship Some 3
Facial hemiplegia Interprets True Movement Inferred relationship Some 3

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Reference Sets

Observable entity foundation reference set

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