FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	autosomal dominant nocturnal frontal lobe epilepsy	ID (Ontology)	DOID:0060681 (Human Disease)
Definition	A frontal lobe epilepsy that is characterized by autosomal dominant inheritance with childhood onset of clusters of brief nocturnal motor seizures with hyperkinetic or tonic manifestations.
Also Known As	"ENFL"
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available

Spanning Tree (Parents/Children)

autosomal genetic disease
 |__autosomal dominant disease__
focal epilepsy                  |
 |__frontal lobe epilepsy_______|
                                autosomal dominant nocturnal frontal lobe epilepsy  12 rec.
                                 |__autosomal dominant nocturnal frontal lobe epilepsy 1 5 rec.
                                 |__autosomal dominant nocturnal frontal lobe epilepsy 2
                                 |__autosomal dominant nocturnal frontal lobe epilepsy 3 1 rec.
                                 |__autosomal dominant nocturnal frontal lobe epilepsy 4 4 rec.
                                 |__autosomal dominant nocturnal frontal lobe epilepsy 5 6 rec.

Spanning Tree View Settings
Parents/Children View Depth	Show hierarchy levels: for parents, for children
Relationships
Is a	autosomal dominant disease frontal lobe epilepsy
Part of
Synonyms & Secondary IDs
Synonyms
	"ENFL" EXACT OMO:0003012
Secondary IDs

External Crossreferences & Linkouts
	GARD:11918 MESH:C579932 MIM:PS600513 ORDO:98784