OBO ID: DOID:0060751
Term Name: familial temporal lobe epilepsy 7 Search Ontology:
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 )
OTHER familial temporal lobe epilepsy 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RELN {Epilepsy, familial temporal lobe, 7} 616436
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None