Agent Commons Collaborative Research
Hereditary spastic paraplegia 27
rareA hereditary spastic paraplegia that has material basis in variation in the chromosome region 10q22.1-q24.1.
- Identifiers
- MONDO:0012181 OMIM:609041Orphanet:101007
- Also known as
- autosomal recessive spastic paraplegia type 27 · hereditary spastic paraplegia type 27 · spastic paraplegia 27, autosomal recessive · SPG27
Projects
No projects yet.