FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

230388003: benigne occipitale epilepsie Gastaut-type (aandoening)

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
3701671010 Benign childhood occipital epilepsy, Gastaut type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5382449016 COVE - childhood occipital visual epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5382450016 Late onset occipital epilepsy of childhood en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5382451017 Childhood occipital visual epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5382452012 Occipital epilepsy of childhood, Gastaut type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5382453019 Childhood occipital visual epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
12063151000146110 G-ICOE nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12063161000146113 Gastaut type ideopathic childhood occipital epilepsy nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12688731000146119 benigne occipitale epilepsie Gastaut-type (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12740711000146112 benigne occipitale epilepsie Gastaut-type nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3701672015 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood occipital visual epilepsy (disorder) Is a kinderepilepsie met occipitale paroxismen (aandoening) false Inferred relationship Some
Childhood occipital visual epilepsy (disorder) Has definitional manifestation Partial seizure false Inferred relationship Some
Childhood occipital visual epilepsy (disorder) Finding site Occipital lobe structure false Inferred relationship Some
Childhood occipital visual epilepsy (disorder) Occurrence Childhood false Inferred relationship Some
Childhood occipital visual epilepsy (disorder) Has definitional manifestation Seizure false Inferred relationship Some
Childhood occipital visual epilepsy (disorder) Finding site Occipital lobe structure true Inferred relationship Some 1
Childhood occipital visual epilepsy (disorder) Is a epileptische aanval op kinderleeftijd false Inferred relationship Some
Childhood occipital visual epilepsy (disorder) Is a Benign occipital lobe epilepsy (disorder) true Inferred relationship Some
Childhood occipital visual epilepsy (disorder) Occurrence Childhood false Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start