Term Name: | Mitchell syndrome |
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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 ) |