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230418006: Lennox-Gastaut syndrome (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
345281011 Lennox-Gastaut syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
618222015 Lennox-Gastaut syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
6521000172110 syndrome de Lennox-Gastaut fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3385161001000113 Lennox-Gastaut-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lennox-Gastaut syndrome Is a épilepsie généralisée cryptogénique false Inferred relationship Some
Lennox-Gastaut syndrome Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Some 1
Lennox-Gastaut syndrome Has definitional manifestation Seizure false Inferred relationship Some
Lennox-Gastaut syndrome Is a A type of epilepsy characterised by frequent epileptiform activity associated with developmental slowing and often regression on the background of previously normal development. In this type of epilepsy the frequent seizures and/or epileptiform discharges, rather than underlying aetiology is thought to be the only cause of developmental impairment. false Inferred relationship Some
Lennox-Gastaut syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Lennox-Gastaut syndrome Finding site Brain structure true Inferred relationship Some 2
Lennox-Gastaut syndrome Is a A type of epilepsy associated with developmental impairment where the developmental impairment is due to both the underlying etiology, independent of epileptic activity, and the superimposed epileptic encephalopathy. An epileptic encephalopathy is where the epileptic activity itself contributes to severe cognitive and behavioral impairments above and beyond what might be expected from the underlying pathology alone. true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Cryptogenic Lennox-Gastaut syndrome Is a True Lennox-Gastaut syndrome Inferred relationship Some
Symptomatic Lennox-Gastaut syndrome Is a True Lennox-Gastaut syndrome Inferred relationship Some

This concept is not in any reference sets

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