← Back to Conditions

Juvenile absence epilepsy

disorder
SNOMED 230413002CUI C4317339

Overview

Juvenile absence 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.

EEG: spike and multispike waves, 3-4 hz
Very frequent (80-99%)HP:0002392
Generalised-onset seizure
Very frequent (80-99%)HP:0002197
Generalized tonic-clonic seizure (without specification of onset)
Very frequent (80-99%)HP:0002069
Abnormal mouth
Frequent (30-79%)HP:0000153
Eye movement issue
Frequent (30-79%)HP:0000496
Generalized non-motor (absence) seizure
Frequent (30-79%)HP:0002121
Jerking
Frequent (30-79%)HP:0001336
Abnormal emotion processing
Occasional (5-29%)HP:0100851
Anxiety disease
Occasional (5-29%)HP:0000739
Febrile seizure (within the age range of 3 months to 6 years)
Occasional (5-29%)HP:0002373
Myoclonic seizure
Occasional (5-29%)HP:0032794
Prolonged seizure
Occasional (5-29%)HP:0002133
Specific learning disability
Occasional (5-29%)HP:0001328

Quick Facts

SNOMED CT
230413002
UMLS CUI
C4317339
Fully Specified Name
Juvenile absence epilepsy (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
13
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.