developmental and epileptic encephalopathy 3 (DOID:0080440)
Alliance: disease page
Synonyms: early infantile epileptic encephalopathy 3
Alt IDs: OMIM:609304
Definition: A developmental and epileptic encephalopathy characterized by onset in the first months of life of erratic, typically myoclonic, refractory seizures that has_material_basis_in homozygous or compound heterozygous mutation in the SLC25A22 gene on chromosome 11p15.