developmental and epileptic encephalopathy, 24

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Print

Disease Overview

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the HCN1 gene.


Synonyms

  • DEE24
  • EIEE24
  • HCN1 early infantile epileptic encephalopathy
  • developmental and epileptic encephalopathy 24
  • early infantile epileptic encephalopathy caused by mutation in HCN1
  • epileptic encephalopathy, early infantile, 24
  • epileptic encephalopathy, early infantile, type 24DEE24
  • EIEE24
  • HCN1 early infantile epileptic encephalopathy
  • developmental and epileptic encephalopathy 24
  • early infantile epileptic encephalopathy caused by mutation in HCN1
  • epileptic encephalopathy, early infantile, 24
  • epileptic encephalopathy, early infantile, type 24