71831005: Symptomatic generalized epilepsy (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

119333016 Symptomatic generalized epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

501972012 Symptomatic generalised epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

501973019 Secondary generalized epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

501974013 Secondary generalised epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

812041018 Symptomatic generalized epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Symptomatic generalized epilepsy	Is a	A type of epilepsy with only generalised onset epileptic seizures.	false	Inferred relationship	Some
Symptomatic generalized epilepsy	Is a	Tonic-clonic epilepsy	false	Inferred relationship	Some
Symptomatic 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	Some	1
Symptomatic generalized epilepsy	Has definitional manifestation	Seizure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Early infantile epileptic encephalopathy with suppression bursts	Is a	False	Symptomatic generalized epilepsy	Inferred relationship	Some
Symptomatic myoclonic epilepsy	Is a	False	Symptomatic generalized epilepsy	Inferred relationship	Some
Myoclonic encephalopathy	Is a	False	Symptomatic generalized epilepsy	Inferred relationship	Some
Pitt-Hopkins syndrome	Has definitional manifestation	False	Symptomatic generalized epilepsy	Inferred relationship	Some
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation is a rare intellectual disability and epilepsy syndrome characterized by global developmental delay and mild to profound intellectual disability, multiple types of usually intractable focal and generalized seizures with variable abnormal EEG findings, and bilateral progressive parenchymal volume loss and thin corpus callosum on brain MRI.	Is a	False	Symptomatic generalized epilepsy	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)