230386004: Childhood epilepsy with occipital paroxysms (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

345233016 Benign occipital epilepsy of childhood en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

345234010 BCEOP - Benign childhood epilepsy with occipital paroxysms en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

345235011 Childhood epilepsy with occipital paroxysms en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618186014 Childhood epilepsy with occipital paroxysms (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1671671000005116 epilepsi i barndommen med occipitale paroksysmer 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 i barndommen med occipitale paroksysmer	Is a	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.	false	Inferred relationship	Some
epilepsi i barndommen med occipitale paroksysmer	Has definitional manifestation	Partial seizure	false	Inferred relationship	Some
epilepsi i barndommen med occipitale paroksysmer	Finding site	Occipital lobe structure	false	Inferred relationship	Some	2
epilepsi i barndommen med occipitale paroksysmer	Occurrence	Childhood	false	Inferred relationship	Some	1
epilepsi i barndommen med occipitale paroksysmer	Has definitional manifestation	Seizure	false	Inferred relationship	Some
epilepsi i barndommen med occipitale paroksysmer	Is a	Finding of head region	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare genetic neurological disorder characterised by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalised convulsion. Autonomic status epilepticus may be the only clinical event in some cases.	Is a	False	epilepsi i barndommen med occipitale paroksysmer	Inferred relationship	Some
A rare genetic neurological disorder with characteristics of childhood to mid-adolescence onset of frequent, brief, diurnal simple partial seizures which usually begin with visual hallucinations (e.g. phosphenes) and/or ictal blindness and may associate non visual seizures (such as deviation of the eyes, oculo clonic seizures), forced eyelid closure and blinking and sensory hallucinations. Post-ictal headache is common while impairment of consciousness is rare.	Is a	False	epilepsi i barndommen med occipitale paroksysmer	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)