has material basis in autosomal recessive disease developmental and epileptic encephalopathy 106 MIM:620028 disease_ontology A developmental and epileptic encephalopathy characterized by onset of various types of frequent seizures within the first year of life and profound global developmental delay with limited ability to move and absent speech that has_material_basis_in homozygous mutation in the UFSP2 gene on chromosome 4q35. DEE106 DOID:0070392 early infantile epileptic encephalopathy 106 developmental and epileptic encephalopathy autosomal recessive inheritance