19598007: Generalized epilepsy (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Seizure\Seizure disorder\Epilepsy\Generalized epilepsy
\Head finding (finding)\Finding of brain\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy

\Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Generalized epilepsy
\Central nervous system finding\Finding of brain\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy

\Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy\Generalized epilepsy

\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy
\Disease\Disorder of head (disorder)\Disorder of brain\Seizure disorder\Epilepsy\Generalized epilepsy

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Generalized epilepsy	Is a	Epilepsy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
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
Generalized epilepsy	Has definitional manifestation	Seizure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Generalized epilepsy	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
épilepsie généralisée cryptogénique	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Generalized nonconvulsive epilepsy	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Idiopathic generalized epilepsy	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Self-limited neonatal epilepsy	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
épilepsie généralisée convulsive	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
épilepsie symptomatique	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
epilessia generalizzata non convulsiva	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Genetic epilepsy with febrile seizures plus (disorder)	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Generalized epilepsy and paroxysmal dyskinesia syndrome (disorder)	Is a	True	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
A type of epilepsy characterized 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 etiology is thought to be the only cause of developmental impairment.	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder)	Is a	True	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Refractory myoclonic epilepsy	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
West syndrome	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Epilepsy with myoclonic absence presents with daily myoclonic absence seizures between 1 to 12 years of age. Other generalized seizure types which may be seen in this syndrome include generalized tonic-clonic seizures, clonic, atonic and typical absence seizures. Developmental impairment may be present at onset of epilepsy and may become more evident with age. The electroencephalogram shows regular three Hz generalized spike-and-wave pattern time-locked with myoclonic jerks, with a normal background.	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Progressive myoclonic epilepsy (disorder)	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Myoclonic epilepsy with ragged red fibers (disorder)	Is a	True	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Benign adult familial myoclonic epilepsy (BAFME) is an inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional generalized or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia.	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial infantile myoclonic epilepsy (disorder)	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Epilepsy with myoclonic-atonic seizures (disorder)	Is a	False	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)
Genetic generalized epilepsy	Is a	True	Generalized epilepsy	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
32997016	Generalized epilepsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
479713017	Generalised epilepsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
747894014	Generalized epilepsy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5180631015	A type of epilepsy with only generalised onset epileptic seizures.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5180632010	A type of epilepsy with only generalized onset epileptic seizures.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
32997016	Generalized epilepsy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
32997016	Generalized epilepsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
479713017	Generalised epilepsy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
479713017	Generalised epilepsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
747894014	Generalized epilepsy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
747894014	Generalized epilepsy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5180631015	A type of epilepsy with only generalised onset epileptic seizures.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5180632010	A type of epilepsy with only generalized onset epileptic seizures.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
924721000195118	epilessia generalizzata	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
876071000195118	Generalisierte Epilepsie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4441000172111	épilepsie généralisée	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4441000172111	épilepsie généralisée	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
924721000195118	epilessia generalizzata	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
876071000195118	Generalisierte Epilepsie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module