765093009: Rolandic epilepsy, speech dyspraxia syndrome (disorder)

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

\Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Focal epilepsy\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\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\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Finding of head and neck region\Head finding (finding)\...

\Finding of brain\Seizure\Seizure disorder\Epilepsy\Focal epilepsy\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Finding of brain\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome (disorder)

\Disorder of head (disorder)\Disorder of brain (disorder)\Seizure disorder\Epilepsy\Focal epilepsy\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\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\Finding of functional performance and activity\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\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\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 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)\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\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\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\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Congenital disease (disorder)\Rolandic epilepsy, speech dyspraxia syndrome (disorder)
\Disease\Idiopathic disease\Localization-related idiopathic epilepsy\Benign Rolandic epilepsy\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

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

4186021000052112 syndrom med rolandisk epilepsi och taldyspraxi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Is a	Benign Rolandic epilepsy	true	Inferred relationship	Some
Rolandic epilepsy, speech dyspraxia syndrome (disorder)	Is a	Congenital disease (disorder)	true	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

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
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
4186021000052112	syndrom med rolandisk epilepsi och taldyspraxi	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)