230390002: Localization-related symptomatic epilepsy (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Aug 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

345239017 Localisation-related symptomatic epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

345240015 Localization-related symptomatic epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618191010 Localization-related symptomatic epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1807351000005114 lokalisationsrelateret symptomgivende epilepsi da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
lokalisationsrelateret symptomgivende epilepsi	Is a	A type of epilepsy with only focal onset epileptic seizures. Seizures can arise from a single location or multiple locations.	false	Inferred relationship	Some
lokalisationsrelateret symptomgivende epilepsi	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
lokalisationsrelateret symptomgivende epilepsi	Has definitional manifestation	Seizure	false	Inferred relationship	Some
lokalisationsrelateret symptomgivende epilepsi	Finding site	Brain structure	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A type of focal epilepsy where all the seizures originate within the temporal lobe.	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
A type of focal epilepsy where all the seizures originate within the mesiobasal limbic area of the temporal lobe.	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
Rasmussen syndrome	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
A type of focal epilepsy where all the seizures originate within the amygdalo-hippocampal area of the temporal lobe.	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
rinencefal epilepsi	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
A type of focal epilepsy where all the seizures originate within the frontal lobe.	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
A type of focal epilepsy where all the seizures originate within the cingulate area of the frontal lobe.	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
A type of focal epilepsy where all the seizures originate within the parietal lobe.	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
Occipital lobe epilepsy	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
kronisk progredierende epilepsia partialis continua i barndommen	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
Ekstratemporal epilepsi	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some
Familial focal epilepsy with variable foci is a rare genetic epilepsy disorder characterized by autosomal dominant lesional and nonlesional focal epilepsy with variable penetrance. Focal seizures emanate from different cortical locations (temporal, frontal, centroparietal, parietal, occipital) in different family members, but for each individual a single focus remains constant throughout lifetime. Seizure type (tonic, tonic-clonic or hyperkinetic) and severity varies among family members and tends to decrease (but do not disappear) during adulthood. Many patients have an aura and show automatisms during diurnal seizures whereas others have nocturnal seizures. Most individuals are of normal intelligence but patients with intellectual disability, autistic spectrum disorder and obsessive-compulsive disorder have been described.	Is a	False	lokalisationsrelateret symptomgivende epilepsi	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)