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192965001: Spastic tetraplegia (disorder)


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
297242010 Spastic tetraplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
576802016 Spastic tetraplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2967583017 Spastic quadriplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
297242010 Spastic tetraplegia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
297242010 Spastic tetraplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
576802016 Spastic tetraplegia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
576802016 Spastic tetraplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2967583017 Spastic quadriplegia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2967583017 Spastic quadriplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
830471000241114 tétraplégie spastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
830471000241114 tétraplégie spastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spastic tetraplegia (disorder) Is a Quadriplegia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Spastic tetraplegia (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Spastic tetraplegia (disorder) Finding site Limb structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spastic tetraplegia (disorder) Is a Disorder of limb true Inferred relationship Existential restriction modifier (core metadata concept)
Spastic tetraplegia (disorder) Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spastic tetraplegia (disorder) Is a Spastic syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Spastic tetraplegia (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
Spastic tetraplegia (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic tetraplegia (disorder) Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Quadriplegic spastic cerebral palsy Is a False Spastic tetraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome Is a True Spastic tetraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Inherited congenital spastic tetraplegia (disorder) Is a True Spastic tetraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) Is a True Spastic tetraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare autosomal ichthyosis syndrome with prominent neurologic signs characterized by the association of congenital ichthyosis with global developmental delay, intellectual disability, infantile-onset seizures, and spastic tetraplegia. Brain imaging may show delayed myelination and cerebral atrophy. Marked intrafamilial variability has been reported. Is a True Spastic tetraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare leukodystrophy characterized by a spectrum of progressive neurologic manifestations comprising rapidly progressive early-onset nystagmus, spastic tetraplegia, and visual and hearing impairment, resulting in death in early childhood, as well as later onset of slowly progressive complex spastic ataxia with pyramidal and cerebellar symptoms and loss of developmental milestones. Brain imaging shows diffuse hypomyelination of the subcortical and deep white matter, cerebellar atrophy, and diffuse spinal cord volume loss. Is a True Spastic tetraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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