Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
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
On this page
- 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.