230435005: Epilepsy undetermined whether focal or generalized (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

345308016 Epilepsy undetermined whether focal or generalised en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

345309012 Epilepsy undetermined whether focal or generalized en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618241017 Epilepsy undetermined whether focal or generalized (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4242531000005115 epilepsi, ikke fastslået om fokal eller generaliseret 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
epilepsi, ikke fastslået om fokal eller generaliseret	Is a	A disease of the brain characterized by an enduring predisposition to generate epileptic seizures.	false	Inferred relationship	Some
epilepsi, ikke fastslået om fokal eller generaliseret	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
epilepsi, ikke fastslået om fokal eller generaliseret	Has definitional manifestation	Seizure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A genetic epilepsy of childhood with characteristics of drug-resistant seizures often induced by fever, presenting in previously healthy children, and which frequently leads to cognitive and motor impairment. Seizures can regress in adulthood but most patients have ongoing seizures that are refractory to medication. Around 85% of cases are due to a mutation or deletion in the SCN1A gene (2q24.3), encoding a voltage-gated sodium channel essential for the excitability of neurons. In families with a known SCN1A mutation, inheritance is autosomal dominant.	Is a	False	epilepsi, ikke fastslået om fokal eller generaliseret	Inferred relationship	Some
Epilepsy with continuous spike wave during slow-wave sleep	Is a	False	epilepsi, ikke fastslået om fokal eller generaliseret	Inferred relationship	Some
A sudden paroxysm of abnormal motor and/or non-motor phenomenon with or without electrographic correlate, or a neonatal electrographic-only seizure (without clinical correlate) that occurs during the period from birth until 44 weeks postmenstrual age.	Is a	False	epilepsi, ikke fastslået om fokal eller generaliseret	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)