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
Related Conditions
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.