Mitchell syndrome

MONDO:0030073

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.

Also known as: ACOX1 upregulation, MITCH, Mitchell syndrome

26 clinical trials for this condition and its sub-types.

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