Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
OMIM:615476 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18; DEE18


In Disease Ontology (DO):
DOID:0050709 - Ohtahara syndrome

In Mondo Disease Ontology:
MONDO:0014201 - early infantile epileptic encephalopathy without suppression burst

Human Disease Resources: OMIM

Xenbase Genes: szt2, c1orf84