developmental and epileptic encephalopathy 28

Summary
Synonym
  • DEE28
  • early infantile epileptic encephalopathy 28
Definition
A developmental and epileptic encephalopathy characterized by onset in the first months of life of refractory seizures, severe axial hypotonia, and profoundly impaired psychomotor development that has_material_basis_in homozygous or compound heterozygous mutation in the WWOX gene on chromosome 16q23.
Super Class
autosomal recessive disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0080452
Mondo Disease Ontology
OMIM
The Human Phenotype Ontology
Displaying entries 21 - 30 of 48 in total
HPO ID HPO Term
HP:0002059 Cerebral atrophy
HP:0001290 Generalized hypotonia
HP:0002355 Difficulty walking
HP:0001337 Tremor
HP:0001257 Spasticity
HP:0002020 Gastroesophageal reflux
HP:0001273 Abnormal corpus callosum morphology
HP:0002317 Unsteady gait
HP:0001336 Myoclonus
HP:0002376 Developmental regression
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

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024