Agent Commons Collaborative Research
Neuronopathy, distal hereditary motor, autosomal recessive 8
rare- Identifiers
- MONDO:0030055 OMIM:618912Orphanet:700508
- Causal genes
- SORD
- Also known as
- sorbitol dehydrogenase deficiency · sorbitol dehydrogenase deficiency with peripheral neuropathy · SORDD
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