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ADNFLE - Autosomal dominant nocturnal frontal lobe epilepsy
disorderSNOMED 698021005CUI C3696898
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Nocturnal seizures
Very frequent (80-99%)HP:0031951
Episodic dystonia
Frequent (30-79%)HP:0002268
Involuntary movements
Frequent (30-79%)HP:0004305
Repetitive behaviour Stereotypic behaviour
Frequent (30-79%)HP:0000733
Depression
Occasional (5-29%)HP:0000716
EEG with focal spikes
Occasional (5-29%)HP:0011193
Excessive, persistent worry and fear
Occasional (5-29%)HP:0000739
Increased theta frequency activity in EEG
Occasional (5-29%)HP:0031535
Intellectual impairment
Occasional (5-29%)HP:0100543
Interictal epileptiform activity
Occasional (5-29%)HP:0011182
Localized hyperkinetic seizure
Occasional (5-29%)HP:0011174
Rapid breathing
Occasional (5-29%)HP:0002883
Sleep walking
Occasional (5-29%)HP:0025236
Suicidal ideation
Occasional (5-29%)HP:0031589
Urinary incontinence
Occasional (5-29%)HP:0000020
Behavioural/Psychiatric abnormality
Very rare (1-4%)HP:0000708
Childhood attention deficit/hyperactivity disorder
Very rare (1-4%)HP:0007018
Generalized tonic-clonic seizure (without specification of onset)
Very rare (1-4%)HP:0002069
Mental retardation, mild
Very rare (1-4%)HP:0001256
NREM parasomnia
Very rare (1-4%)HP:0025235
Psychotic mentation
Very rare (1-4%)HP:0001345
Quick Facts
- SNOMED CT
- 698021005
- UMLS CUI
- C3696898
- Fully Specified Name
- Familial sleep-related hypermotor 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.