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36803009: Idiopathic generalized epilepsy (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
61389013 Idiopathic generalized epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
486556017 Idiopathic generalised epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768598012 Idiopathic generalized epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160677019 IGE - idiopathic generalized epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160679016 IGE - idiopathic generalised epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160676011 A distinct sub-group of genetic generalised epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalised tonic-clonic seizures alone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160678012 A distinct sub-group of genetic generalized epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalized tonic-clonic seizures alone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
61389013 Idiopathic generalized epilepsy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
61389013 Idiopathic generalized epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
486556017 Idiopathic generalised epilepsy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
486556017 Idiopathic generalised epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768598012 Idiopathic generalized epilepsy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
768598012 Idiopathic generalized epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1216513011 Primary generalised epilepsy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216513011 Primary generalised epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1218003019 Primary generalized epilepsy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1218003019 Primary generalized epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160677019 IGE - idiopathic generalized epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160679016 IGE - idiopathic generalised epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160676011 A distinct sub-group of genetic generalised epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalised tonic-clonic seizures alone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160678012 A distinct sub-group of genetic generalized epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalized tonic-clonic seizures alone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
225751000172115 épilepsie généralisée idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
225751000172115 épilepsie généralisée idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic generalized epilepsy Is a Generalized epilepsy false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic generalized epilepsy Is a épilepsie tonicoclonique false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic generalized epilepsy 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 Existential restriction modifier (core metadata concept) 1
Idiopathic generalized epilepsy Has definitional manifestation Seizure false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic generalized epilepsy Is a Genetic generalized epilepsy true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic generalized epilepsy Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Myoclonic epilepsy in infancy Is a False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited familial neonatal epilepsy Is a False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Benign non-familial neonatal convulsions (disorder) Is a False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
épilepsie myoclonique de la petite enfance Is a False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Juvenile absence epilepsy Is a True Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Epilepsy with generalised tonic-clonic seizures alone Is a True Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Childhood absence epilepsy Is a True Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Juvenile myoclonic epilepsy Is a True Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Primäre generalisierte Absence-Epilepsie Is a False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Status epilepticus due to generalized idiopathic epilepsy Due to False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept) 1
Refractory idiopathic generalized epilepsy Is a False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)
Jeavons syndrome Is a False Idiopathic generalized epilepsy Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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