Autosomal dominant epilepsy with auditory features

disorder

SNOMED 784377008CUI C1838062

Overview

Autosomal dominant epilepsy with auditory features is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

EEG with focal epileptiform discharges

Very frequent (80-99%)HP:0011185

Focal seizures

Very frequent (80-99%)HP:0007359

Hearing sounds

Very frequent (80-99%)HP:0008765

Difficulty finding words

Frequent (30-79%)HP:0002381

Focal auditory seizure

Frequent (30-79%)HP:0011158

Focal autonomic seizure with epigastric sensation/nausea/vomiting/other gastrointestinal phenomena

Frequent (30-79%)HP:0011159

Focal aware sensory seizure with auditory features

Frequent (30-79%)HP:0032864

Interictal epileptiform activity

Frequent (30-79%)HP:0011182

Localized dyscognitive seizure

Frequent (30-79%)HP:0002384

Autonomic dysregulation

Occasional (5-29%)HP:0012332

Cephalic aura

Occasional (5-29%)HP:0032810

Deja vu aura

Occasional (5-29%)HP:0012005

Focal automatism seizure

Occasional (5-29%)HP:0032898

Focal autonomic seizure with palpitations/tachycardia/bradycardia/asystole

Occasional (5-29%)HP:0032773

Focal autonomic seizures

Occasional (5-29%)HP:0011154

Focal clonic seizure

Occasional (5-29%)HP:0002266

Focal seizure without impairment of awareness

Occasional (5-29%)HP:0002349

Nocturnal seizures

Occasional (5-29%)HP:0031951

Partial olfactory seizure

Occasional (5-29%)HP:0011161

Partial vestibular seizure

Occasional (5-29%)HP:0032759

Simple partial occipital seizures

Occasional (5-29%)HP:0011165

Visual hallucination

Occasional (5-29%)HP:0002367

Behavioral changes

Very rare (1-4%)HP:0000708

Depressive episode

Very rare (1-4%)HP:0000716

Generalised-onset seizure

Very rare (1-4%)HP:0002197

Generalized tonic-clonic seizure (without specification of onset)

Very rare (1-4%)HP:0002069

Impulsivity

Very rare (1-4%)HP:0100710

Intermittent migraine headaches

Very rare (1-4%)HP:0002076

Secondary generalized tonic clonic seizures

Very rare (1-4%)HP:0007334

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Epilepsy with auditory features(parent)

Familial temporal lobe epilepsy(parent)

Quick Facts

SNOMED CT: 784377008
UMLS CUI: C1838062
Fully Specified Name: Familial epilepsy with auditory features (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 29

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.