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1230018005: Corticobasal syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5066421019 Corticobasal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066422014 Corticobasal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400106018 A rare neurologic disease characterized by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400107010 A rare neurologic disease characterised by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5066421019 Corticobasal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066422014 Corticobasal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066423016 A rare neurologic disease with characteristics of multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia and visuospatial dysfunction. The disease shows a wide clinical variability between patients with many developing a relatively pure motor syndrome, and others displaying a combination of motor and cognitive deficits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400106018 A rare neurologic disease characterized by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400107010 A rare neurologic disease characterised by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3388081001000114 Kortikobasales Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3388081001000114 Kortikobasales Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Corticobasal syndrome (disorder) Is a Disorder of cerebral cortex (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Corticobasal syndrome (disorder) Is a Parkinsonism true Inferred relationship Existential restriction modifier (core metadata concept)
Corticobasal syndrome (disorder) Is a Cerebral degeneration (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Corticobasal syndrome (disorder) Is a Chronic brain syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Corticobasal syndrome (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 4
Corticobasal syndrome (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 3
Corticobasal syndrome (disorder) Has interpretation Slow true Inferred relationship Existential restriction modifier (core metadata concept) 3
Corticobasal syndrome (disorder) Finding site Basal ganglion structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Corticobasal syndrome (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Corticobasal syndrome (disorder) Finding site Cerebral cortex true Inferred relationship Existential restriction modifier (core metadata concept) 2
Corticobasal syndrome (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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