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 1 - 10 of 55 in total
HPO ID HPO Term
HP:0002521 Hypsarrhythmia
HP:0001336 Myoclonus
HP:0012469 Infantile spasms
HP:0000707 Abnormality of the nervous system
HP:0011121 Abnormal skin morphology
HP:0002376 Developmental regression
HP:0000054 Micropenis
HP:0000070 Ureterocele
HP:0000110 Renal dysplasia
HP:0000175 Cleft palate
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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Last updated: December 9, 2024