765093009: Rolandic epilepsy, speech dyspraxia syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Central nervous system finding\Finding of brain\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Seizure\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Finding of brain\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Disorder of head\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Functional finding\Communication disorder\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome
• \Functional finding\Finding of functional performance and activity\Developmental disorder of motor function\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome
• \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
• \Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Communication disorder\Speech and language disorder\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Disorder of head\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Congenital disease\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Idiopathic disease\Localisation-related idiopathic epilepsy\Benign Rolandic epilepsy\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Developmental disorder\Neurodevelopmental disorder\Developmental disorder of motor function\Speech and language dyspraxias\Rolandic epilepsy, speech dyspraxia syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Rolandic epilepsy, speech dyspraxia syndrome

Status: current, Primitive. 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	Case sensitive	SNOMED CT core
3656385015	Rolandic epilepsy, speech dyspraxia syndrome	en	Synonym	Active	Case sensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Queensland allied health indicator for intervention reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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