Benign familial neonatal-infantile seizures

disorder

SNOMED 1231282002CUI C5671283

Overview

Benign familial neonatal-infantile seizures 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 spikes

Frequent (30-79%)HP:0011193

Focal clonic seizure

Frequent (30-79%)HP:0002266

Generalized tonic-clonic seizure (without specification of onset)

Frequent (30-79%)HP:0002069

Neonatal seizure

Frequent (30-79%)HP:0032807

Tonic seizure

Frequent (30-79%)HP:0032792

Abnormal retropulsion test

Occasional (5-29%)HP:0002172

Apnea

Occasional (5-29%)HP:0002104

Dizziness

Occasional (5-29%)HP:0002321

Headache

Occasional (5-29%)HP:0002315

Nausea

Occasional (5-29%)HP:0002018

Paroxysmal ataxia

Occasional (5-29%)HP:0002131

Slurred speech

Occasional (5-29%)HP:0001350

Staring gaze

Occasional (5-29%)HP:0025401

Electrical status epilepticus during slow-wave sleep

Very rare (1-4%)HP:0031491

Intellectual deterioration

Very rare (1-4%)HP:0001268

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Self-limited focal epilepsy(parent)

Quick Facts

SNOMED CT: 1231282002
UMLS CUI: C5671283
Fully Specified Name: Self-limited familial neonatal-infantile epilepsy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.