Familial temporal lobe epilepsy

disorder

SNOMED 783739005CUI C1842564

Overview

Familial temporal lobe epilepsy 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.

Febrile status epilepticus

Frequent (30-79%)HP:0032656

Febrile seizure (within the age range of 3 months to 6 years)

HP:0002373

Focal seizure without impairment of awareness

HP:0002349

Generalized tonic-clonic seizure (without specification of onset)

HP:0002069

Localized dyscognitive seizure

HP:0002384

Related Conditions

Benign familial mesial temporal lobe epilepsy(child)

Autosomal dominant epilepsy with auditory features(child)

Familial disease(parent)

Genetic disease(parent)

Temporal lobe epilepsy(parent)

Quick Facts

SNOMED CT: 783739005
UMLS CUI: C1842564
Fully Specified Name: Familial temporal lobe epilepsy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.