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familial partial epilepsy - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

familial partial epilepsy

MONDO:0017704

Also known as:familial focal epilepsyhereditary partial epilepsyepilepsy, partial, familial

Overview

An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.

Diagnosis

Biomarker and diagnostic research for familial partial epilepsy has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for familial partial epilepsy.

85 publications have been identified in PubMed for familial partial epilepsy. Research spans Case Report / Case Series (33%), Basic Science / Preclinical (29%), and Review / Meta-Analysis (12%).

Research Type	Count	% of Total
Patient case studies	28	33%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 5:30 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:309

GARD

Genetic and Rare Diseases Info Center

GARD:2173

Questions for Your Care Team

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familial partial epilepsy

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications