765093009: syndrome d'épilepsie rolandique-dyspraxie de la parole (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 idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\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 idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\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 idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\constatation à propos l'encéphale\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\affection de la tête\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\constatation fonctionnelle\trouble de communication\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\constatation fonctionnelle\Finding of functional performance and activity\troubles du développement d'une fonction motrice\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\constatation à propos de la parole\Speech and language finding\constatation à propos de la communication, de l'élocution et du langage\trouble de communication\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Neurological finding\Seizure related finding\convulsion\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\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 idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\trouble de communication\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\affection de la tête\Disorder of brain (disorder)\trouble convulsif\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Congenital disease\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\maladie idiopathique\Localisation-related idiopathic epilepsy\épilepsie rolandique bénigne (trouble)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\trouble du développement\Neurodevelopmental disorder\troubles du développement d'une fonction motrice\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\trouble du développement\Developmental hereditary disorder\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3656383010 Rolandic epilepsy, speech dyspraxia syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3656385015 Rolandic epilepsy, speech dyspraxia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
767571000241117 syndrome d'épilepsie rolandique-dyspraxie de la parole (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
871851000172115 syndrome d'épilepsie rolandique-dyspraxie de la parole fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3656384016 Rare genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3656386019 Rare genetic epilepsy characterised by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalised childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed. 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
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	interprète (attribut)	capacité d'exécuter les fonctions reliées à la communication	true	Inferred relationship	Some	2
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	2
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	3
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	est un(e) (attribut)	épilepsie rolandique bénigne (trouble)	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	est un(e) (attribut)	Congenital disease	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	est un(e) (attribut)	Speech and language dyspraxias	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	est un(e) (attribut)	Hereditary disorder of nervous system	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	localisation d'une constatation (attribut)	structure du cerveau	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3656383010	Rolandic epilepsy, speech dyspraxia syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3656385015	Rolandic epilepsy, speech dyspraxia syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
767571000241117	syndrome d'épilepsie rolandique-dyspraxie de la parole (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
871851000172115	syndrome d'épilepsie rolandique-dyspraxie de la parole	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3656384016	Rare genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3656386019	Rare genetic epilepsy characterised by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalised childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core