OBO ID: DOID:0060752
Term Name: familial temporal lobe epilepsy 5 Search Ontology:
Synonyms:
  • ETL5
Definition: A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13. https://www.ncbi.nlm.nih.gov/pubmed/21922598
References:
Ontology: Human Disease   (DOID:0060752)
OTHER familial temporal lobe epilepsy 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CPA6 Epilepsy, familial temporal lobe, 5 614417
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None