Search Ontology:
Human Disease

familial temporal lobe epilepsy 5

Term ID
DOID:0060752
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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