developmental and epileptic encephalopathy 74

Summary
Synonym
  • DEE74
  • early infantile epileptic encephalopathy 74
Definition
A developmental and epileptic encephalopathy characterized by onset in the first months of life of refractory seizures and severe global developmental delay with hypotonia, severe motor impairment, roving eye movements, and absent language that has_material_basis_in heterozygous mutation in the GABRG2 gene on chromosome 5q34.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
External Links
Disease Ontology
DOID:0112210
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2566 GABRG2 gamma-aminobutyric acid type A receptor subunit gamma2
Displaying 1 entry
Gene ID Gene Symbol Description Source
14406 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
29709 Gabrg2 gamma-aminobutyric acid type A receptor subunit gamma 2
The Human Phenotype Ontology
Displaying entries 1 - 10 of 48 in total
HPO ID HPO Term
HP:0000648 Optic atrophy
HP:0000504 Abnormality of vision
HP:0000750 Delayed speech and language development
HP:0000348 High forehead
HP:0000708 Atypical behavior
HP:0001250 Seizure
HP:0000546 Retinal degeneration
HP:0000252 Microcephaly
HP:0000639 Nystagmus
HP:0000717 Autism
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: August 19, 2024