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Rolandic epilepsy, speech dyspraxia syndrome
disorderSNOMED 765093009CUI C4707308
Overview
Rolandic epilepsy, speech dyspraxia 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.
Seizures
Very frequent (80-99%)HP:0001250
Speech difficulties
Very frequent (80-99%)HP:0000750
Verbal dyspraxia
Very frequent (80-99%)HP:0011098
EEG with focal sharp waves
Frequent (30-79%)HP:0011196
EEG with generalized epileptiform discharges
Frequent (30-79%)HP:0011198
Electrical status epilepticus during slow-wave sleep
Frequent (30-79%)HP:0031491
Focal seizures
Frequent (30-79%)HP:0007359
Mental deficiency
Frequent (30-79%)HP:0001249
Secondary generalized tonic clonic seizures
Frequent (30-79%)HP:0007334
Sialorrhea
Frequent (30-79%)HP:0002307
Abnormal prosody
Occasional (5-29%)HP:0031434
Difficulty articulating speech
Occasional (5-29%)HP:0001260
Hypoplasia of corpus callosum
Occasional (5-29%)HP:0002079
Incomprehensible speech
Occasional (5-29%)HP:0002546
Low pitched voice
Occasional (5-29%)HP:0010300
Nasal speech
Occasional (5-29%)HP:0001611
Poor attention span
Occasional (5-29%)HP:0000736
Specific learning disability
Occasional (5-29%)HP:0001328
Quick Facts
- SNOMED CT
- 765093009
- UMLS CUI
- C4707308
- Fully Specified Name
- Rolandic epilepsy, speech dyspraxia syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.