Search Ontology:
Human Disease

familial focal epilepsy with variable foci 3

Term ID
DOID:0081423
Synonyms
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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