OBO ID: DOID:0060748
Term Name: familial temporal lobe epilepsy 1 Search Ontology:
Synonyms:
  • ETL1
  • partial epilepsy with auditory features
Definition: A temporal lobe epilepsy characterized by autosomal dominant inheritance of partial seizures originating from the temporal lobe that are often accompanied by auditory symptoms and that has_material_basis_in heterozygous mutation in the LGI1 gene on chromosome 10q24. (3)
References:
Ontology: Human Disease   ( DOID:0060748 )
Relationships
is a type of:
OTHER familial temporal lobe epilepsy 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LGI1 Epilepsy, familial temporal lobe, 1 600512
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)
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