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716278005: Epilepsy with eyelid myoclonia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3305371019 Jeavons syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5173082010 Epilepsy with eyelid myoclonia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5173083017 Epilepsy with eyelid myoclonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5173091014 EEM - epilepsy with eyelid myoclonia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5232445013 A type of epilepsy that presents between 2 and 14 years of age with the triad of frequent eyelid myoclonia, with or without absences, induced by eye closure and photic stimulation. Eyelid myoclonia is often most prominent on awakening. Generalized tonic-clonic seizures occur in the majority of cases but are usually infrequent. The electroencephalogram shows bursts of 3 to 6 Hz generalized spike-wave or polyspike-and-wave which are often triggered by eye closure and/or photic stimulation, with a normal background. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5232446014 A type of epilepsy that presents between 2 and 14 years of age with the triad of frequent eyelid myoclonia, with or without absences, induced by eye closure and photic stimulation. Eyelid myoclonia is often most prominent on awakening. Generalised tonic-clonic seizures occur in the majority of cases but are usually infrequent. The electroencephalogram shows bursts of 3 to 6 Hz generalised spike-wave or polyspike-and-wave which are often triggered by eye closure and/or photic stimulation, with a normal background. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
889921000172111 EMEA - eyelid myoclonia with and without absences fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
1011451000172111 syndrome de Jeavons fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
891061000172116 Jeavons-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
938161000172113 syndroom van Jeavons nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epilepsy with eyelid myoclonia (disorder) Is a Idiopathic generalized epilepsy false Inferred relationship Some
Epilepsy with eyelid myoclonia (disorder) Is a Reflex epilepsy false Inferred relationship Some
Epilepsy with eyelid myoclonia (disorder) Finding site Cerebrum false Inferred relationship Some 1
Epilepsy with eyelid myoclonia (disorder) Has definitional manifestation Seizure false Inferred relationship Some
Epilepsy with eyelid myoclonia (disorder) Is a Genetic generalised epilepsy true Inferred relationship Some
Epilepsy with eyelid myoclonia (disorder) Finding site Brain structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian subset for medical problems in patient health records

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