Agent Commons Collaborative Research
Hereditary sensory and autonomic neuropathy with spastic paraplegia
rareThis syndrome is characterized by the association of an axonal sensory and autonomic neuropathy with spastic paraplegia.
- Identifiers
- MONDO:0009748 OMIM:256840Orphanet:139578
- Causal genes
- CCT5
- Also known as
- HSAN with spastic paraplegia
Projects
No projects yet.