developmental and epileptic encephalopathy neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy early-infantile DEE https://github.com/monarch-initiative/mondo/issues/8274 https://github.com/monarch-initiative/mondo/issues/8454 https://github.com/monarch-initiative/mondo/issues/8557 https://www.epilepsydiagnosis.org/syndrome/eme-overview.html ICD9:345.6 early myoclonic encephalopathy with suppression-bursts MONDO:0800491 UMLS:C0393706 DOID:0050709 myoclonia epileptica myoclonic seizure disorder epileptic encephalopathy, infantile MEDGEN:97959 DOID:2481 A neonatal/infantile epilepsy syndrome characterized by frequent drug-resistant seizures that begin ≤3 months of age, with abnormal interictal EEG and neurological examination. In up to 80% of patients, EIDEE is caused by an underlying structural, genetic, or metabolic reason. epileptic seizures, myoclonic SCTID:230429005 myoclonus epilepsy infantile epileptic encephalopathy MedDRA:10071545 NCIT:C116593 SCTID:44423001 early infantile epileptic encephalopathy with suppression-bursts EIDEE early myoclonic encephalopathy epileptic seizures - myoclonic early infantile epileptic encephalopathy myoclonic seizure DOID:308 early-infantile developmental and epileptic encephalopathy syndrome GARD:0027299 Orphanet:1935 Ohtahara syndrome Orphanet:1934 myoclonic epilepsy epileptic encephalopathy, early infantile EIEE icd11.foundation:1877241469 EME