developmental and epileptic encephalopathy 99

Summary
Synonym
  • DEE99
  • early infantile epileptic encephalopathy 99
Definition
A developmental and epileptic encephalopathy characterized by onset of seizures in early childhood that has_material_basis_in heterozygous mutation in the ATP1A3 gene on chromosome 19q13.
Super Class
autosomal dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0070385
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
232975 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
Displaying 1 entry
Gene ID Gene Symbol Description Source
24213 Atp1a3 ATPase Na+/K+ transporting subunit alpha 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
48971 Atpalpha Na pump alpha subunit
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