Search Ontology:
Human Disease
familial focal epilepsy with variable foci 3
- Term ID
- DOID:0081423
- Synonyms
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- Definition
- A familial focal epilepsy with variable foci that has_material_basis_in heterozygous mutation in the NPRL3 gene on chromosome 16p13. https://pubmed.ncbi.nlm.nih.gov/26505888/
- References
- Ontology
- Human Disease ( DOID:0081423 )
- is a type of
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