familial temporal lobe epilepsy 1

Summary
Synonym
  • 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.
Super Class
autosomal dominant disease temporal lobe epilepsy
Disease Ontology
DOID:0060748
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9211 LGI1 leucine rich glioma inactivated 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
56839 Lgi1 leucine-rich repeat LGI family, member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
252892 Lgi1 leucine-rich, glioma inactivated 1

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024