Search Ontology:
Human Disease

familial temporal lobe epilepsy 7

Term ID
DOID:0060751
Synonyms
  • ETL7
Definition
A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has_material_basis_in heterozygous mutation in the RELN gene on chromosome 7q22. https://www.ncbi.nlm.nih.gov/pubmed/26046367
References
Ontology
Human Disease   ( DOID:0060751 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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