784377008: Autosomal dominant epilepsy with auditory features (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Central nervous system finding\Finding of brain\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Seizure\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Finding of brain\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Finding of head region\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Disorder of head\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant epilepsy with auditory features
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant epilepsy with auditory features
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant epilepsy with auditory features
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Autosomal dominant epilepsy with auditory features
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Disease\Disorder of head\Encephalopathy\Seizure disorder\Epilepsy\Localisation-related epilepsy\Localisation-related symptomatic epilepsy\Temporal lobe epilepsy\Autosomal dominant epilepsy with auditory features
• \Disease\Familial disease\Autosomal dominant epilepsy with auditory features

Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3763852010	Partial epilepsy with auditory aura	en	Synonym	Active	Case insensitive	SNOMED CT core
3763853017	Autosomal dominant epilepsy with auditory features (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3763854011	Autosomal dominant epilepsy with auditory features	en	Synonym	Active	Case insensitive	SNOMED CT core
3763855012	Autosomal dominant lateral temporal lobe epilepsy	en	Synonym	Active	Case insensitive	SNOMED CT core
3763856013	A rare genetic familial partial epilepsy disease with characteristics of focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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