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84757009: epilepsie (aandoening)

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

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

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

\Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy

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

178739011 Epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

826667014 Epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

56551000146118 epilepsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

944371000146118 epilepsie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

5180629012 A disease of the brain characterized by an enduring predisposition to generate epileptic seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5180630019 A disease of the brain characterised by an enduring predisposition to generate epileptic seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

11005981000146119 Het aanvalsgewijs, meestal kortdurend, plaatsvinden van veranderingen in de elektrische activiteit van hersencellen, met stoornissen in de hersenfunctie tot gevolg; hierdoor gaat de controle over het lichaam enige tijd verloren; kenmerkend zijn schokkende bewegingen. nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Epilepsy	Is a	Seizure disorder	true	Inferred relationship	Some
Epilepsy	Finding site	Cerebrum	false	Inferred relationship	Some	1
Epilepsy	Has definitional manifestation	Seizure	false	Inferred relationship	Some
Epilepsy	Finding site	Brain structure	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial infantile myoclonic epilepsy	Is a	True	Epilepsy	Inferred relationship	Some
Epilepsy due to congenital infectious disease (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Epilepsy due to glucose transporter protein type 1 deficiency syndrome (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Epilepsy due to Rasmussen syndrome (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Epilepsy due to perinatal intraventricular haemorrhage	Is a	True	Epilepsy	Inferred relationship	Some
Epilepsy due to perinatal cerebral ischemia (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Epilepsy due to perinatal periventricular hemorrhage (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Malignant migrating partial seizures of infancy (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Benign infantile seizure with mild gastroenteritis syndrome (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Developmental and epileptic encephalopathy	Is a	True	Epilepsy	Inferred relationship	Some
Epileptic encephalopathy (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome	Is a	True	Epilepsy	Inferred relationship	Some
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
West syndrome	Is a	True	Epilepsy	Inferred relationship	Some
Progressive myoclonic epilepsy	Is a	True	Epilepsy	Inferred relationship	Some
MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome	Is a	True	Epilepsy	Inferred relationship	Some
Education about epilepsy and driving	Has focus	True	Epilepsy	Inferred relationship	Some	2
Symptomatic epilepsy (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Ketogenic diet for epilepsy	Has focus	True	Epilepsy	Inferred relationship	Some	1
Pre-existing epilepsy in pregnancy (disorder)	Is a	True	Epilepsy	Inferred relationship	Some
Surgical procedure for epilepsy	Has focus	True	Epilepsy	Inferred relationship	Some	2
Benzodiazepine withdrawal epilepsy (disorder)	Is a	True	Epilepsy	Inferred relationship	Some

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Reference Sets

Dutch pathology simple reference set (foundation metadata concept)

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
178739011	Epilepsy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
826667014	Epilepsy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
56551000146118	epilepsie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
944371000146118	epilepsie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
5180629012	A disease of the brain characterized by an enduring predisposition to generate epileptic seizures.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5180630019	A disease of the brain characterised by an enduring predisposition to generate epileptic seizures.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
11005981000146119	Het aanvalsgewijs, meestal kortdurend, plaatsvinden van veranderingen in de elektrische activiteit van hersencellen, met stoornissen in de hersenfunctie tot gevolg; hierdoor gaat de controle over het lichaam enige tijd verloren; kenmerkend zijn schokkende bewegingen.	nl	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)