Hereditary motor and sensory neuropathy type 5
Other Names for this Disease
- CMT with pyramidal features
- Hereditary motor and sensory neuropathy 5
- HMSN 5
- Peroneal muscular atrophy with pyramidal features, autosomal dominant
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- The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.