Search Ontology:
Human Disease

familial temporal lobe epilepsy 2

Term ID
DOID:0060755
Synonyms
  • ETL2
Definition
A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex or partial seizures and childhood febrile seizures that has_material_basis_in variation in the chromosome region 12q22-q23.3. (2)
References
Ontology
Human Disease   ( DOID:0060755 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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