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Standards Ontologies Notations
familial temporal lobe epilepsy 3

Summary
Synonym
  • FMTLE
  • familial mesial temporal lobe epilepsy
Definition
A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has_material_basis_in variation in the chromosome region 4q13.2-q21.3.
Super Class
autosomal dominant disease temporal lobe epilepsy
External Links
Disease Ontology
DOID:0060750
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5243 ABCB1 ATP binding cassette subfamily B member 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
18669 Abcb1b ATP-binding cassette, sub-family B member 1B
18671 Abcb1a ATP-binding cassette, sub-family B member 1A
Displaying all 2 entries
Gene ID Gene Symbol Description Source
36428 Mdr49 Multi drug resistance 49
38726 Mdr65 Multi drug resistance 65
Displaying all 2 entries
Gene ID Gene Symbol Description Source
178215 pgp-1 Multidrug resistance protein pgp-1
181326 pgp-3 Multidrug resistance protein pgp-3
Displaying 1 entry
Gene ID Gene Symbol Description Source
853671 STE6 ATP-binding cassette a-factor transporter STE6
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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

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Last updated: August 19, 2024