hereditary spastic paraplegia
MONDO:0019064Also known as: spastic paraplegia, HSP, SPG, Strümpell-Lorrain disease, familial spastic paraplegia
- MONDO:
- MONDO:0019064
- Orphanet:
- 685 ↗
Rare disease91 associated genes
Description
Hereditary spastic paraplegias (HSP) comprise a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.
Associated genes
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