765093009: syndroom van rolandische epilepsie en spraakdyspraxie (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Seizure\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Functional finding\Motor function\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Functional finding\Communication disorder\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Functional finding\Developmental disorder of motor function\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Speech finding\Speech and language finding\Communication, speech and language finding\Communication disorder\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital neurological disorder (disorder)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Congenital neurological disorder (disorder)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Communication disorder\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Self-limited focal epilepsy\Self-limited epilepsy with centrotemporal spikes\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Developmental disorder\Neurodevelopmental disorder\Developmental disorder of motor function\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Developmental disorder\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

6726451000146116 syndroom van rolandische epilepsie en verbale dyspraxie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6726461000146118 syndroom van rolandische epilepsie en spraakdyspraxie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6726471000146112 syndroom van rolandische epilepsie en spraakdyspraxie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained 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)	Is a	Self-limited epilepsy with centrotemporal spikes	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Is a	Congenital disease (disorder)	false	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Is a	Speech and language dyspraxias	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Finding site	Cerebrum	true	Inferred relationship	Some	1
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Interprets	Ability to perform functions related to communication	true	Inferred relationship	Some	2
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Has interpretation	Abnormal	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)	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Is a	Motor function	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Interprets	Motor function	true	Inferred relationship	Some	4
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Is a	Congenital neurological disorder (disorder)	true	Inferred relationship	Some

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
6726451000146116	syndroom van rolandische epilepsie en verbale dyspraxie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6726461000146118	syndroom van rolandische epilepsie en spraakdyspraxie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6726471000146112	syndroom van rolandische epilepsie en spraakdyspraxie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained 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