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Standards Ontologies Notations
developmental and epileptic encephalopathy

Summary
Definition
An electroclinical syndrome characterized by epileptiform activity and at least one other pathology that together contribute to cognitive and behavioral impairments including developmental delay or regression with onset anywhere from birth to adulthood.
Super Class
electroclinical syndrome
External Links
Disease Ontology
DOID:0112202
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entry 11 - 11 of 11 in total
Gene ID Gene Symbol Description Source
140679 SLC32A1 solute carrier family 32 member 1
Displaying entries 11 - 12 of 12 in total
Gene ID Gene Symbol Description Source
277854 Depdc5 DEP domain containing 5
329777 Pigk phosphatidylinositol glycan anchor biosynthesis, class K
Displaying all 3 entries
Gene ID Gene Symbol Description Source
117559 Sv2a synaptic vesicle glycoprotein 2a
140694 Dnm1 dynamin 1
171146 Kcnh5 potassium voltage-gated channel subfamily H member 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
32428 eag ether a go-go
Displaying 1 entry
Gene ID Gene Symbol Description Source
176431 unc-47 Vesicular GABA transporter
Displaying all 2 entries
Gene ID Gene Symbol Description Source
853603 IML1 GTPase-activating protein IML1
853870 VPS1 dynamin-like GTPase VPS1
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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