developmental and epileptic encephalopathy 66

Summary
Synonym
  • DEE66
  • early infantile epileptic encephalopathy 66
Definition
A developmental and epileptic encephalopathy characterized by onset in the first days or weeks of life of seizures, global developmental delay with hypotonia, behavioral abnormalities, and dysmorphic features or ophthalmologic defects that has_material_basis_in heterozygous mutation in the PACS2 gene on chromosome 14q32.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0080446
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23241 PACS2 phosphofurin acidic cluster sorting protein 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
217893 Pacs2 phosphofurin acidic cluster sorting protein 2
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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