770405003: epilepsie temporale mésiale familiale bénigne (trouble)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du système nerveux central\constatation à propos l'encéphale\convulsion\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy
\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy

\constatation à propos d'une région de la tête et du cou\Head finding (finding)\...

\constatation à propos l'encéphale\convulsion\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy
\constatation à propos l'encéphale\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy

\Finding of head region\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy

\affection de la tête\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy

\Neurological finding\Seizure related finding\convulsion\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Benign familial mesial temporal lobe epilepsy
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Benign familial mesial temporal lobe epilepsy
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Benign familial mesial temporal lobe epilepsy
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Benign familial mesial temporal lobe epilepsy
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy
\Disease\affection de la tête\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Benign familial mesial temporal lobe epilepsy

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3700714010 Benign familial mesial temporal lobe epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3700715011 Benign FMTLE (familial mesial temporal lobe epilepsy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3700716012 Benign familial mesial temporal lobe epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

769231000241113 epilepsie temporale mésiale familiale bénigne (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

891371000172111 epilepsie temporale mésiale familiale bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3700717015 Rare epilepsy with characteristics of seizures with viscerosensory or experiential auras, onset in adolescence or early adulthood and good prognosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign familial mesial temporal lobe epilepsy	est un(e) (attribut)	Temporal lobe epilepsy	true	Inferred relationship	Some
Benign familial mesial temporal lobe epilepsy	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Benign familial mesial temporal lobe epilepsy	est un(e) (attribut)	Hereditary disorder of nervous system	true	Inferred relationship	Some
Benign familial mesial temporal lobe epilepsy	localisation d'une constatation (attribut)	Temporal lobe structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

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Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set