developmental and epileptic encephalopathy 33

Summary
Synonym
  • DEE33
  • early infantile epileptic encephalopathy 33
Definition
A developmental and epileptic encephalopathy characterized by onset in the first months of life of seizures and severe global developmental delay with impaired intellectual development and poor or absent speech that has_material_basis_in heterozygous mutation in the EEF1A2 gene on chromosome 20q13.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0080463
Mondo Disease Ontology
OMIM
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1915 EEF1A1 eukaryotic translation elongation factor 1 alpha 1
1917 EEF1A2 eukaryotic translation elongation factor 1 alpha 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
13627 Eef1a1 eukaryotic translation elongation factor 1 alpha 1
13628 Eef1a2 eukaryotic translation elongation factor 1 alpha 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
175975 eef-1A.1 Elongation factor 1-alpha
181044 eef-1A.2 Elongation factor 1-alpha
The Human Phenotype Ontology
Displaying entries 41 - 48 of 48 in total
HPO ID HPO Term
HP:0007018 Attention deficit hyperactivity disorder
HP:0002421 Poor head control
HP:0010844 EEG with multifocal slow activity
HP:0012447 Abnormal myelination
HP:0002521 Hypsarrhythmia
HP:0100660 Dyskinesia
HP:0004322 Short stature
HP:0011968 Feeding difficulties
Displaying all 5 entries
Gene ID Gene Symbol Description
1759 DNM1 dynamin 1
523 ATP6V1A ATPase H+ transporting V1 subunit A
781 CACNA2D1 calcium voltage-gated channel auxiliary subunit alpha2delta 1
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
8867 SYNJ1 synaptojanin 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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Last updated: December 9, 2024