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434551000124106: Benign childhood epilepsy with centrotemporal spikes, non-refractory (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
    3776387014 Benign rolandic epilepsy, non-refractory en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    634451000124112 Benign childhood epilepsy with centrotemporal spikes, non-refractory (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    634461000124114 Benign childhood epilepsy with centrotemporal spikes, non-refractory en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    634471000124119 Benign childhood epilepsy with centrotemporal spikes, non-intractable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3776387014 Benign rolandic epilepsy, non-refractory en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    634451000124112 Benign childhood epilepsy with centrotemporal spikes, non-refractory (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    634461000124114 Benign childhood epilepsy with centrotemporal spikes, non-refractory en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    634471000124119 Benign childhood epilepsy with centrotemporal spikes, non-intractable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    5798501000241114 épilepsie infantile bénigne non réfractaire avec pointes centrotemporales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    5798501000241114 épilepsie infantile bénigne non réfractaire avec pointes centrotemporales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    épilepsie infantile bénigne non réfractaire avec pointes centrotemporales Is a épilepsie, pas réfractaire false Inferred relationship Existential restriction modifier (core metadata concept)
    épilepsie infantile bénigne non réfractaire avec pointes centrotemporales Is a 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. false Inferred relationship Existential restriction modifier (core metadata concept)
    épilepsie infantile bénigne non réfractaire avec pointes centrotemporales 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) 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    REPLACED BY association reference set (foundation metadata concept)

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