Term Name:	Mitchell syndrome
Synonyms:
Definition:	A peroxisomal disease characterized by progressive episodic demyelination, sensorimotor polyneuropathy, and hearing loss that has_material_basis_in heterozygous mutation in the ACOX1 gene on chromosome 17q25.1.
Ontology:	Human Disease [DOID:0070516]   ( DOID:0070516 )