|  Help  |  About  |  Contact Us

DO Term : familial temporal lobe epilepsy 1 [DOID:0060748] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • partial epilepsy with auditory features,
  • ETL1,
  • ORDO:101046,
  • 600512,
  • OMIM:600512
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents