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15523002: Self-limited focal epilepsy (disorder)

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
5348006019 Self-limited focal epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5348007011 Self-limited focal epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5348008018 SeLFE - self-limited focal epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5362255019 A group of epilepsies characterized by age-dependent occurrence of drug responsive focal seizures in otherwise normal children. Seizures are focal motor or sensory with or without impaired awareness and may evolve to bilateral tonic-clonic seizures. Remission usually occurs by puberty. Development and cognition are typically normal. Neurological examination is normal. No significant structural lesions of the brain are present, and presumed genetic factors have an important role. The electroencephalogram (EEG) background activity is normal. Seizure semiology and EEG features are specific for each of the syndromes included in this group. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5362256018 A group of epilepsies characterised by age-dependent occurrence of drug responsive focal seizures in otherwise normal children. Seizures are focal motor or sensory with or without impaired awareness and may evolve to bilateral tonic-clonic seizures. Remission usually occurs by puberty. Development and cognition are typically normal. Neurological examination is normal. No significant structural lesions of the brain are present, and presumed genetic factors have an important role. The electroencephalogram (EEG) background activity is normal. Seizure semiology and EEG features are specific for each of the syndromes included in this group. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
26317017 Benign focal epilepsy of childhood en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
26317017 Benign focal epilepsy of childhood en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
742361013 Benign focal epilepsy of childhood (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
742361013 Benign focal epilepsy of childhood (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5348006019 Self-limited focal epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5348007011 Self-limited focal epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5348008018 SeLFE - self-limited focal epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5362255019 A group of epilepsies characterized by age-dependent occurrence of drug responsive focal seizures in otherwise normal children. Seizures are focal motor or sensory with or without impaired awareness and may evolve to bilateral tonic-clonic seizures. Remission usually occurs by puberty. Development and cognition are typically normal. Neurological examination is normal. No significant structural lesions of the brain are present, and presumed genetic factors have an important role. The electroencephalogram (EEG) background activity is normal. Seizure semiology and EEG features are specific for each of the syndromes included in this group. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5362256018 A group of epilepsies characterised by age-dependent occurrence of drug responsive focal seizures in otherwise normal children. Seizures are focal motor or sensory with or without impaired awareness and may evolve to bilateral tonic-clonic seizures. Remission usually occurs by puberty. Development and cognition are typically normal. Neurological examination is normal. No significant structural lesions of the brain are present, and presumed genetic factors have an important role. The electroencephalogram (EEG) background activity is normal. Seizure semiology and EEG features are specific for each of the syndromes included in this group. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4440911000241110 épilepsie focale bénigne de l'enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4440911000241110 épilepsie focale bénigne de l'enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

12 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Self-limited focal epilepsy (disorder) Is a epilessia idiopatica correlata a localizzazione false Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited focal epilepsy (disorder) Is a Focal onset epileptic seizure (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited focal epilepsy (disorder) 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) 2
Self-limited focal epilepsy (disorder) Has definitional manifestation Partial seizure false Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited focal epilepsy (disorder) Occurrence Childhood false Inferred relationship Existential restriction modifier (core metadata concept) 1
Self-limited focal epilepsy (disorder) Has definitional manifestation Seizure false Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited focal epilepsy (disorder) Is a Focal epilepsy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited focal epilepsy (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
épilepsie bénigne frontale de l'enfance Is a False Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
épilepsie psychomotrice bénigne de l'enfance Is a False Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Benign atypical partial epilepsy in childhood Is a True Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Epilepsy with recurrent unilateral seizures in children Is a False Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
épilepsie de l'enfance avec paroxysmes occipitaux Is a False Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Recurrent benign focal seizures of childhood Is a False Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A common type of self-limited focal epilepsy syndrome, which begins typically between four and ten years (peak is seven years; range three to twelve years). Seizures are focal, infrequent (most children have fewer than ten in lifetime), brief (typically less than two to three minutes) and occur mostly in sleep (eighty to ninety percent of children). Individuals may have frequent seizures over a few days or weeks and then several months before subsequent seizure. Focal seizures with characteristic frontoparietal opercular features and/or nocturnal bilateral tonic-clonic seizures are mandatory for diagnosis. Characteristic semiology includes somatosensory symptoms (unilateral numbness or paresthesia of the tongue, lips, gums and inner cheek), orofacial motor signs (unilateral tonic or clonic contractions), speech arrest (dysarthria or anarthria) with preserved understanding, and sialorrhea. Seizures may evolve rapidly to tonic-clonic activity of the ipsilateral upper limb, to an ipsilateral hemiclonic seizure, or to a focal to bilateral tonic-clonic seizure. Todd paresis may occur postictally. Seizures occurring during sleep are seen within one hour of falling asleep or one to two hours prior to awakening. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram (EEG) background activity is normal. EEG must show centrotemporal biphasic epileptiform discharges which are characteristically high-amplitude complexes (less than 200 microvolts, peak to trough) that activate in drowsiness and sleep. MRI is normal or has nonspecific findings. Is a True Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited infantile epilepsy (disorder) Is a True Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited neonatal epilepsy Is a True Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited epilepsy with autonomic seizures Is a True Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Self-limited familial neonatal-infantile epilepsy Is a True Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Infantile convulsion and choreoathetosis syndrome (disorder) Is a True Self-limited focal epilepsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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