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221360009: Spasticity (finding)

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
333933014 Muscle spasticity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
333934015 Muscle spasm - tone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
333935019 Muscular spasticity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
333936018 Spasticity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
608155010 Spasticity (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1832961000195114 spasticità it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
347981000077117 spasticité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

20 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spasticity Is a Increased muscle tone true Inferred relationship Some
Spasticity Finding site Skeletal muscle structure true Inferred relationship Some 2
Spasticity Interprets Muscle tone false Inferred relationship Some 1
Spasticity Has interpretation Increased false Inferred relationship Some 1
Spasticity Is a Musculoskeletal finding true Inferred relationship Some
Spasticity Is a General finding of soft tissue true Inferred relationship Some
Spasticity Interprets Muscle tone true Inferred relationship Some 1
Spasticity Has interpretation Increased true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Spastic paraparesis Is a True Spasticity Inferred relationship Some
Clasp knife like increase in tone Is a True Spasticity Inferred relationship Some
On examination - muscle tone spastic Associated finding False Spasticity Inferred relationship Some 1
Spastic paralysis Is a True Spasticity Inferred relationship Some
Spastic paresis (finding) Is a True Spasticity Inferred relationship Some
Lower limb spasticity (finding) Is a True Spasticity Inferred relationship Some
Upper limb spasticity (finding) Is a True Spasticity Inferred relationship Some
Lethal neonatal spasticity Is a False Spasticity Inferred relationship Some
Muscle spasticity of spinal origin (finding) Is a True Spasticity Inferred relationship Some
On examination - muscle tone spastic Is a False Spasticity Inferred relationship Some
Spasticity as sequela of stroke (disorder) Is a True Spasticity Inferred relationship Some
A rare ARX-related epileptic encephalopathy characterized by infantile onset of myoclonic epilepsy with generalized spasticity, severe global developmental delay, and moderate to profound intellectual disability. Obligate female carriers show subtle, generalized hyperreflexia. Late onset progressive spastic ataxia has also been reported. Is a True Spasticity Inferred relationship Some
Microcephaly-brain defect-spasticity-hypernatremia syndrome is a rare congenital genetic syndrome with a central nervous system malformation as a major feature characterized by microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatremia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. There have been no further descriptions in the literature since 1986. Is a True Spasticity Inferred relationship Some
A rare, genetic, neurological disorder characterized by parkinsonian features (including resting or action tremor, cogwheel rigidity, hypomimia and bradykinesia) associated with variably penetrant spasticity, hyperactive deep tendon reflexes and Babinski sign. Is a True Spasticity Inferred relationship Some
Childhood-onset spasticity with hyperglycinemia is a rare neurometabolic disease characterized by a childhood onset of progressive spastic ataxia associated with gait disturbances, hyperreflexia, extensor plantar responses and non-ketotic hyperglycinemia typically revealed by biochemical analysis. Additional signs of upper extremity spasticity, dysarthria, learning difficulties, poor concentration, nystagmus, optic atrophy and reduced visual acuity may also be associated. Is a False Spasticity Inferred relationship Some
Dynamic ileus Due to False Spasticity Inferred relationship Some 2
Spastic ileus of the newborn Due to False Spasticity Inferred relationship Some 2
A rare genetic neurological disorder characterized by neonatal onset of rigidity and intractable seizures, with episodic jerking already beginning in utero. Affected infants have small heads, remain visually inattentive, do not feed independently, and make no developmental progress. Frequent spontaneous apnea and bradycardia usually culminate in cardiopulmonary arrest and death in infancy, although some cases were described with a milder clinical course and survival into childhood. Is a True Spasticity Inferred relationship Some
Spastic miosis (disorder) Due to True Spasticity Inferred relationship Some 3
A rare genetic neurodegenerative disorder characterized by congenital microphthalmia, sunken eyes, blindness, microcephaly, severe intellectual disability, progressive spasticity, and seizures. Psychomotor development is normal in the first 6-8 months of life and thereafter declines rapidly and continuously. Brain MRI reveals progressive and extensive degenerative changes, especially cortex, cerebellum, brainstem, and corpus callosum atrophy, with complete loss of cerebral white matter. Is a True Spasticity Inferred relationship Some
Spastic ataxia (finding) Is a True Spasticity Inferred relationship Some

This concept is not in any reference sets

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