DO_rare_slim has material basis in autosomal recessive disease developmental and epileptic encephalopathy 23 DOID:0080415 A developmental and epileptic encephalopathy characterized by onset in the first months of life of intractable seizures, severely impaired psychomotor development with poor or absent speech, cortical blindness, and dysmorphic facial features that has_material_basis_in homozygous or compound heterozygous mutation in the DOCK7 gene on chromosome 1p31. DEE23 Epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome disease_ontology Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome MIM:615859 ORDO:411986 early infantile epileptic encephalopathy 23 developmental and epileptic encephalopathy autosomal recessive inheritance