Benign familial mesial temporal lobe epilepsy

disorder

SNOMED 770405003CUI C1968848

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Deja vu aura

Very frequent (80-99%)HP:0012005

Localized dyscognitive seizure

Frequent (30-79%)HP:0002384

Secondary generalized tonic clonic seizures

Frequent (30-79%)HP:0007334

Related Conditions

Hereditary disorder of nervous system(parent)

Familial temporal lobe epilepsy(parent)

MTLE - mesial temporal lobe epilepsy(parent)

Quick Facts

SNOMED CT: 770405003
UMLS CUI: C1968848
Fully Specified Name: Familial mesial temporal lobe epilepsy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 3

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.