has material basis in autosomal dominant disease developmental and epileptic encephalopathy developmental and epileptic encephalopathy 73 disease_ontology A developmental and epileptic encephalopathy characterized by onset in the months of life of refractory seizures, profound developmental delay, failure to thrive, hypotonia, and are unable to walk, speak, or feed properly that has_material_basis_in heterozygous mutation in the RNF13 gene on chromosome 3q25.1. MIM:618379 DEE73 DOID:0112209 early infantile epileptic encephalopathy 73 autosomal dominant inheritance