Benign myoclonic epilepsy in infancy

disorder

SNOMED 192990004CUI C0751120

Overview

Benign myoclonic epilepsy in infancy 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.

Childhood attention deficit/hyperactivity disorder

Very frequent (80-99%)HP:0007018

EEG with irregular generalised spike and wave complexes

Very frequent (80-99%)HP:0001326

Generalized tonic-clonic seizure (without specification of onset)

Very frequent (80-99%)HP:0002069

Mental retardation, mild

Very frequent (80-99%)HP:0001256

Myoclonic epilepsy, progressive

Very frequent (80-99%)HP:0002123

Aggression

Frequent (30-79%)HP:0000718

Incoordination

Frequent (30-79%)HP:0002311

Intellectual deterioration

Frequent (30-79%)HP:0001268

Involuntary jerking movements

Frequent (30-79%)HP:0001336

Irritability

Frequent (30-79%)HP:0000737

Mental and motor retardation

Frequent (30-79%)HP:0001263

Poor hand-eye coordination

Frequent (30-79%)HP:0007057

Psychomotor regression beginning in infancy

Frequent (30-79%)HP:0002376

Delayed fine motor development

Occasional (5-29%)HP:0010862

Difficulty articulating speech

Occasional (5-29%)HP:0001260

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

Occasional (5-29%)HP:0002373

Generalized non-motor (absence) seizure

Occasional (5-29%)HP:0002121

Language impairment

Occasional (5-29%)HP:0002463

Leber optic atrophy

Occasional (5-29%)HP:0001112

Photically induced tonic-clonic seizure

Occasional (5-29%)HP:0007207

Paralysis on one side of body

Very rare (1-4%)HP:0002301

Related Conditions

Genetic generalised epilepsy(parent)

Quick Facts

SNOMED CT: 192990004
UMLS CUI: C0751120
Fully Specified Name: Myoclonic epilepsy in infancy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 21

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.