developmental and epileptic encephalopathy, 31A https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/7641 https://github.com/monarch-initiative/mondo/issues/8019 https://www.malacards.org/card/developmental_and_epileptic_encephalopathy_31a DNM1 early infantile epileptic encephalopathy DEE31 early infantile epileptic encephalopathy caused by mutation in DNM1 UMLS:C4225357 DNM1-encephalopathy and neurodevelopmental disorder GARD:0016094 Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene. OMIM:616346 DNM1-related epilepsy and neurodevelopmental disorder epileptic encephalopathy, early infantile, 31 developmental and epileptic encephalopathy 31A, autosomal dominant MEDGEN:894942 epileptic encephalopathy, early infantile, type 31 DEE31A DOID:0080437 MONDO:0014598 developmental and epileptic encephalopathy 31 EIEE31 Lennox-Gastaut syndrome undetermined early-onset epileptic encephalopathy neonatal-onset developmental and epileptic encephalopathy DNM1-encephalopathy and neurodevelopmental disorder