Term Name:	encephalopathy due to defective mitochondrial and peroxisomal fission 1
Synonyms:
Definition:	A syndrome that has_material_basis_in heterozygous mutation in the DNM1L gene, and is characterized by delayed psychomotor development and has_symptom hypotonia that may lead to death in childhood.
Ontology:	Human Disease [DOID:0070347]   ( DOID:0070347 )