developmental and epileptic encephalopathy 9

Summary
Synonym
  • DEE9
  • EFMR
  • EIEE9
  • Juberg Hellman syndrome
  • early infantile epileptic encephalopathy 9
  • early infantile female-limited epilecptic encephalopathy
  • female restricted epilepsy with mental retardation
Definition
A developmental and epileptic encephalopathy characterized by seizure onset in infancy and mild to severe intellectual impairment in females that has_material_basis_in heterozygous mutation in the gene encoding protocadherin-19 (PCDH19) on chromosome Xq22.
Super Class
X-linked dominant disease developmental and epileptic encephalopathy
Disease Ontology
DOID:0060848
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
57526 PCDH19 protocadherin 19
Displaying 1 entry
Gene ID Gene Symbol Description Source
279653 Pcdh19 protocadherin 19
Displaying 1 entry
Gene ID Gene Symbol Description Source
555688 pcdh19 protocadherin 19

About Release Notes Help Feedback

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