Overview
Doose syndrome 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 spike waves
Very frequent (80-99%)HP:0011197
Generalised myoclonic-atonic seizure
Very frequent (80-99%)HP:0011170
Bilateral tonic-clonic seizure with generalized onset
Frequent (30-79%)HP:0025190
Childhood attention deficit/hyperactivity disorder
Frequent (30-79%)HP:0007018
EEG: spike and multispike waves, 3-4 hz
Frequent (30-79%)HP:0002392
Eyelid myoclonus
Frequent (30-79%)HP:0025097
Generalized non-motor (absence) seizure
Frequent (30-79%)HP:0002121
Hyperactive behaviour
Frequent (30-79%)HP:0000752
Lack of peer relationships
Frequent (30-79%)HP:0002332
Myoclonic epilepsy, progressive
Frequent (30-79%)HP:0002123
Poor school performance
Frequent (30-79%)HP:0001249
Sudden loss of muscle tone
Frequent (30-79%)HP:0010819
Abnormal emotion processing
Occasional (5-29%)HP:0100851
Ataxia
Occasional (5-29%)HP:0001251
Autism spectrum disorder
Occasional (5-29%)HP:0000729
Brain imaging abnormality
Occasional (5-29%)HP:0410263
Cobb angle greater than ten degrees
Occasional (5-29%)HP:0002650
Delayed CNS myelination
Occasional (5-29%)HP:0002188
EEG with irregular generalised spike and wave complexes
Occasional (5-29%)HP:0001326
EEG: generalized slow activity
Occasional (5-29%)HP:0010845
Interictal epileptiform activity
Occasional (5-29%)HP:0011182
Myoclonic seizure
Occasional (5-29%)HP:0032794
Reduced social responsiveness
Occasional (5-29%)HP:0012760
Simple febrile seizures
Occasional (5-29%)HP:0011171
Tremor
Occasional (5-29%)HP:0001337
Abnormally small eyeball
Very rare (1-4%)HP:0000568
Bulging forehead
Very rare (1-4%)HP:0011220
Central hypotonia
Very rare (1-4%)HP:0001252
Corticospinal signs
Very rare (1-4%)HP:0007256
Decreased size of cranium
Very rare (1-4%)HP:0000252
Quick Facts
- SNOMED CT
- 230421008
- UMLS CUI
- C0393702
- Fully Specified Name
- Epilepsy with myoclonic-atonic seizures (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.