developmental and epileptic encephalopathy 30

Summary
Synonym
  • DEE30
  • early infantile epileptic encephalopathy 30
Definition
A developmental and epileptic encephalopathy characterized by onset in the first few months of life of refractory seizures andseverely impaired or absent developmental progress that has_material_basis_in heterozygous mutation in the SIK1 gene on chromosome 21q22.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0080465
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
150094 SIK1 salt inducible kinase 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
850785 KIN2 serine/threonine protein kinase KIN2
851700 KIN1 serine/threonine protein kinase KIN1
The Human Phenotype Ontology
Displaying entries 31 - 40 of 55 in total
HPO ID HPO Term
HP:0002069 Bilateral tonic-clonic seizure
HP:0002079 Hypoplasia of the corpus callosum
HP:0002121 Generalized non-motor (absence) seizure
HP:0002131 Episodic ataxia
HP:0002353 EEG abnormality
HP:0002360 Sleep abnormality
HP:0002373 Febrile seizure (within the age range of 3 months to 6 years)
HP:0002421 Poor head control
HP:0002506 Diffuse cerebral atrophy
HP:0005280 Depressed nasal bridge
Displaying all 5 entries
Gene ID Gene Symbol Description
23236 PLCB1 phospholipase C beta 1
51227 PIGP phosphatidylinositol glycan anchor biosynthesis class P
5277 PIGA phosphatidylinositol glycan anchor biosynthesis class A
6487 ST3GAL3 ST3 beta-galactoside alpha-2,3-sialyltransferase 3
9091 PIGQ phosphatidylinositol glycan anchor biosynthesis class Q

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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