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Standards Ontologies Notations
autosomal dominant nocturnal frontal lobe epilepsy 5

Summary
Synonym
  • ENFL5
  • nocturnal frontal lobe epilepsy 5
Definition
An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34.
Super Class
autosomal dominant nocturnal frontal lobe epilepsy
Disease Ontology
DOID:0060686
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
57582 KCNT1 potassium sodium-activated channel subfamily T member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
227632 Kcnt1 potassium channel, subfamily T, member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
60444 Kcnt1 potassium sodium-activated channel subfamily T member 1
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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: December 9, 2024