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Neuronopathy, distal hereditary motor, autosomal recessive 8

MONDO:0030055

Also known as: SORDD, sorbitol dehydrogenase deficiency, sorbitol dehydrogenase deficiency with peripheral neuropathy

17 clinical trials for this condition and its sub-types, 2 tagged with Neuronopathy, distal hereditary motor, autosomal recessive 8 itself.

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