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Childhood absence epilepsy

disorder
SNOMED 50866000CUI C4281785

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.

EEG with spike-wave complexes (2.5-3.5 Hz)
Very frequent (80-99%)HP:0010848
Typical absence seizures
Very frequent (80-99%)HP:0011147
Childhood attention deficit/hyperactivity disorder
Frequent (30-79%)HP:0007018
Paleness
Frequent (30-79%)HP:0000980
Abnormal social interactions
Occasional (5-29%)HP:0012433
Depressive episode
Occasional (5-29%)HP:0000716
Dyslexia
Occasional (5-29%)HP:0010522
Excessive, persistent worry and fear
Occasional (5-29%)HP:0000739
Febrile seizure (within the age range of 3 months to 6 years)
Occasional (5-29%)HP:0002373
Generalized tonic-clonic seizure (without specification of onset)
Occasional (5-29%)HP:0002069
Impaired visuospatial constructive cognition
Occasional (5-29%)HP:0010794
Mental deficiency
Occasional (5-29%)HP:0001249
Myoclonic absences
Occasional (5-29%)HP:0011150
Punding
Occasional (5-29%)HP:0030218
Rapid breathing
Occasional (5-29%)HP:0002883
Specific learning disability
Occasional (5-29%)HP:0001328
Uncontrolled eye movements
Occasional (5-29%)HP:0007738
Worthlessness
Occasional (5-29%)HP:0031469
Jerky head movements
Very rare (1-4%)HP:0006961
Myoclonus of limbs
Very rare (1-4%)HP:0045084
Urinary incontinence
Very rare (1-4%)HP:0000020

Quick Facts

SNOMED CT
50866000
UMLS CUI
C4281785
Fully Specified Name
Childhood absence epilepsy (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.