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Hereditary spastic paraplegia 16
rareA hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq11.2.
- Identifiers
- MONDO:0010287 OMIM:300266Orphanet:100997
- Part of
- Hereditary spastic paraplegia
- Also known as
- hereditary spastic paraplegia type 16 · spastic paraplegia 16 · spastic paraplegia 16, X-linked · spastic paraplegia 16, X-linked, complicated, X-linked recessive · SPG16
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