FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	familial focal epilepsy with variable foci	ID (Ontology)	DOID:0081420 (Human Disease)
Definition	A focal epilepsy that is characterized by focal seizures, with seizure onset in a discrete area of the brain including the temporal, frontal, parietal, and occipital lobes, with focal seizures arising from different cortical regions in different family members.
Also Known As	"DEPDC5-related epilepsy"
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
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Spanning Tree (Parents/Children)

autosomal genetic disease
 |__autosomal dominant disease__
epilepsy                        |
 |__focal epilepsy______________|
                                familial focal epilepsy with variable foci  11 rec.
                                 |__familial focal epilepsy with variable foci 1 4 rec.
                                 |__familial focal epilepsy with variable foci 2 3 rec.
                                 |__familial focal epilepsy with variable foci 3 3 rec.
                                 |__familial focal epilepsy with variable foci 4 1 rec.

Spanning Tree View Settings
Parents/Children View Depth	Show hierarchy levels: for parents, for children
Relationships
Is a	autosomal dominant disease focal epilepsy
Part of
Synonyms & Secondary IDs
Synonyms
	"DEPDC5-related epilepsy" EXACT
Secondary IDs

External Crossreferences & Linkouts
	GARD:13295 MIM:PS604364 ORDO:98820