developmental and epileptic encephalopathy 43

Summary
Synonym
  • DEE43
  • early infantile epileptic encephalopathy 43
Definition
A developmental and epileptic encephalopathy characterized by onset in the first year of life of seizures, global developmental delay, and mild to moderate intellectual disability that has_material_basis_in heterozygous mutation in the GABRB3 gene on chromosome 15q11.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0080447
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2562 GABRB3 gamma-aminobutyric acid type A receptor subunit beta3
Displaying 1 entry
Gene ID Gene Symbol Description Source
14402 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
24922 Gabrb3 gamma-aminobutyric acid type A receptor subunit beta 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
32554 Lcch3 Ligand-gated chloride channel homolog 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
176691 gab-1 Gamma-aminobutyric acid receptor subunit beta
The Human Phenotype Ontology
Displaying entries 11 - 20 of 25 in total
HPO ID HPO Term
HP:0000741 Apathy
HP:0002321 Vertigo
HP:0000708 Atypical behavior
HP:0001336 Myoclonus
HP:0007270 Atypical absence seizure
HP:0000718 Aggressive behavior
HP:0011195 EEG with focal sharp slow waves
HP:0000752 Hyperactivity
HP:0002353 EEG abnormality
HP:0012758 Neurodevelopmental delay
Displaying 1 entry
Gene ID Gene Symbol Description
1759 DNM1 dynamin 1

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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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